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Masters Degrees (Drug Safety)

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The aim of this MSc is to provide a postgraduate education in pharmacovigilance, including relevant techniques, the basis of adverse drug reactions, regulations and guidelines, handling safety issues including labelling and risk management and systems and processes. Read more
The aim of this MSc is to provide a postgraduate education in pharmacovigilance, including relevant techniques, the basis of adverse drug reactions, regulations and guidelines, handling safety issues including labelling and risk management and systems and processes. Teaching consists of lectures and workshop activities in small groups and takes into account real world situations. There are opportunities for sharing experiences and networking which contributes to the development of your knowledge and understanding of pharmacovigilance issues.

Flexible programme

This is a flexible programme designed to meet the needs of those in either full or part-time employment who are likely to have a spread of responsibilities. Students are able to complete the MSc course in under three years if able to attend all modules at the earliest opportunity. Alternatively, they can take up to five years, progressing at a slower pace.

Participants will normally be graduates and/or experienced personnel and usually will need to have held positions in drug safety for one to several years. The programme is run as a series of intensive short courses supplemented with substantial pre and post-course reading and set coursework. In addition, if you are studying for an MSc, you will undertake a research project that is normally carried out at your workplace but may be done at the University, or an institution with appropriate experience of pharmacovigilance or adverse drug reactions.

The programme has attracted students from European Union countries, Norway, Switzerland, Japan and the USA and its success has led to the organisation of an annual Pharmacovigilance Update day for those who have completed their studies.

Recruitment will take place at the beginning of each taught module and the programme offers the awards of a PgC, PgD or MSc. Students are typically able to obtain any one of the awards in a minimum of two years; however you have a maximum registration of up to five years in order to complete the course. This course has the option of being a diploma if you do not feel you can commit to the full MSc programme.

Why choose this course?

-The MSc/PgD/PgC in Pharmacovigilance is a programme developed by the School of Life and Medical Sciences and the Pharmaceutical Information and Pharmacovigilance Association (PIPA).
-In addition to offering this course, The University of Hertfordshire is also part of the Eu2P European Programme in Pharmacovigilance and Pharmacoepidemiology, an online pan European e-learning/e-teaching MSc course.
-The programme includes eight taught modules, provided as intensive three-day workshops, and for the MSc award, a research project.
-It is taught mainly through teams of staff drawn from the professions appropriate to pharmacovigilance. This is a major feature of the programme, the majority of staff delivering the courses will be acknowledged experts.
-The aim is to provide a postgraduate education in pharmacovigilance, including relevant techniques, the basis of adverse drug reactions, regulations and guidelines, handling safety issues and the role of systems and processes.

Professional Accreditations

PIPA (Pharmaceutical Information and Pharmacovigilance Association)

Careers

Potential candidates will normally be in either full or part-time employment and are likely to have a spread of responsibilities, mostly in pharmacovigilance and medical information, monitoring safety data in either pre- and post-marketing studies or from spontaneous reports. They will be graduates and/or experienced personnel and usually will have held positions in drug safety for one to several years. Some applicants may have doctorates and may be medically qualified. Following successful completion of the course the knowledge gained should enable the post-graduates to make a greater contribution to the pharmacovigilance industry.

Teaching methods

Taught modules normally consist of approximately 24 hours class contact. In addition, about 120 hours will be needed to complete the pre and post-course activities. The actual amount of time spent will depend upon your existing knowledge and ability. All modules are free-standing. Satisfactory completion of four modules is compulsory for the PgCert; all eight modules are required for the PgDip and MSc. Coursework will contribute significantly to assessment and may comprise some or all of the following: summaries of pre-course reading, written reports of class discussions, essays, performances in seminars, poster presentations, problem solving or data interpretation exercise, short projects and case studies. Unseen written examinations will feature in some courses; they may be used to examine understanding of pre-course reading material. Attendance at the taught component and satisfactory completion of both coursework and examinations (where present), with a minimum mark of 50% in each element, is normally required to pass each module.

Structure

Year 1
Optional
-Adverse Drug Reactions by Major Body Systems I
-Adverse Drug Reactions by Major Body Systems II
-Drug Safety in Clinical Trials
-Labelling and Risk Management
-Management of Pharmacovigilance Data
-Pharmacoepidemiology
-Pharmacovigilance Regulations and Guidelines
-Principles of Pharmacovigilance

Year 2
Optional
-Adverse Drug Reactions by Major Body Systems I
-Adverse Drug Reactions by Major Body Systems II
-Drug Safety in Clinical Trials
-Labelling and Risk Management
-Management of Pharmacovigilance Data
-Pharmacoepidemiology
-Pharmacovigilance Regulations and Guidelines
-Principles of Pharmacovigilance

Year 3
Optional
-Adverse Drug Reactions by Major Body Systems I
-Adverse Drug Reactions by Major Body Systems II
-Drug Safety in Clinical Trials
-Labelling and Risk Management
-Management of Pharmacovigilance Data
-Pharmacoepidemiology
-Pharmacovigilance Regulations and Guidelines
-Principles of Pharmacovigilance
-Project, Pharmacovigilance

Year 4
Optional
-Adverse Drug Reactions by Major Body Systems I
-Adverse Drug Reactions by Major Body Systems II
-Drug Safety in Clinical Trials
-Labelling and Risk Management
-Management of Pharmacovigilance Data
-Pharmacoepidemiology
-Pharmacovigilance Regulations and Guidelines
-Principles of Pharmacovigilance
-Project, Pharmacovigilance

Year 5
Optional
-Adverse Drug Reactions by Major Body Systems I
-Adverse Drug Reactions by Major Body Systems II
-Drug Safety in Clinical Trials
-Labelling and Risk Management
-Management of Pharmacovigilance Data
-Pharmacoepidemiology
-Pharmacovigilance Regulations and Guidelines
-Principles of Pharmacovigilance
-Project, Pharmacovigilance

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This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process. Read more

This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.

It addresses key aspects of preclinical drug evaluation through the study of:

  • Drug discovery and development
  • Safety pharmacology
  • Mechanisms of drug-induced toxicities
  • Regulatory affairs
  • Bioanalytical sciences

It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.

As part of the programme you will undertake an original research project that will be the basis of your dissertation.

Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.

Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.

Rankings

Top 200 - 2018 QS World University Rankings by subject.

"The course contains the perfect balance between theoretical learning in lectures and hands-on experience by putting our theoretical learning into practice. It has helped spark a greater in-depth interest and knowledge into science and science-related research."

Manisha Prabhakar, MSc Drug Toxicology and Safety Pharmacology

What you will study

The programme delivers a combination of theoretical learning and hands-on laboratory experience in a number of key aspects of biomedical, pharmacological and toxicological laboratory techniques.

Key elements of scientific analysis, such as critical appraisal and analysis and presentation of data, are also included.

Core Modules

Option Modules

Learning and assessment

You'll learn through lectures, tutorials, student-led seminars and laboratory investigation, plus self-directed learning.

Assessment consists of exams and coursework. An important component is the final dissertation derived from the research project.

Career prospects

The programme gives you the skills you need for a career in the pharmaceutical industry, clinical trials, or regulatory bodies, along with the foundations for PhD study.

Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.

The majority of our students find employment in the pharmaceutical industry (e.g. Covance, Envigo, Cyprotex) as well as the clinical setting ( e.g clinical trials at St James Hospital, Leeds). A number of overseas students have returned to their country of origin and have taken high profile positions in the regulatory environment. In addition, many of our students have continued their education and progressed to PhD study (e.g. Universities of Oxford, Leeds, Liverpool, and Bradford).

The University is committed to helping students develop and enhance employability and this is an integral part of many programmes. Specialist support is available throughout the course from Career and Employability Services including help to find part-time work while studying, placements, vacation work and graduate vacancies. Students are encouraged to access this support at an early stage and to use the extensive resources on the Careers website.

Discussing options with specialist advisers helps to clarify plans through exploring options and refining skills of job-hunting. In most of our programmes there is direct input by Career Development Advisers into the curriculum or through specially arranged workshops.



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This course is one of our three specialist pharmacy MSc courses (Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics). Read more
This course is one of our three specialist pharmacy MSc courses (Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics).

You’ll gain a thorough understanding and awareness of your chosen area of pharmacy, the research methods required to complete a final supervised research project and an overview of the drug discovery process.

These courses are primarily designed to prepare you for an academic or industrial career in the relevant area. You may be a scientist already working within the pharmaceutical industry or a recent science graduate.

You will undertake a variety of compulsory modules and a research project. This project will last approximately four months and you will work under the supervision of recognised experts in their field. The project allows you to undertake a detailed investigation and develop practical expertise in a specialist pharmaceutical sciences area. The University also has strong links with numerous pharmaceutical companies - there may be the opportunity to undertake your project in collaboration with one of these companies.

Pharmacokinetics is a key aspect of drug safety and investigates the fate of a drug in the body, and how the substance is absorbed, distributed, metabolised and eliminated. Develop your skill and knowledge in the application of pharmacokinetics to the design and optimisation of new therapeutics. This course has been developed with an emphasis on describing mechanistic approaches to assessing and predicting the pharmacokinetics of drugs throughout the drug development process. You will encounter a broad range of experiences in the application of pharmacokinetics from early discovery and development, through to market authorisation and clinical applications.

What you will study

All students studying one of our three pharmacy MSc courses will take the following core modules:
-Research Methods 1: Professional Development
-Research Methods 2: Communication Skills
-Research Project
-Drug Discovery

Depending upon the course you chose, you will also undertake the following modules:
-Chemotherapy & Selective Toxicity
-Drug Dosage Form & Design
-Pharmacology

Learning, teaching & assessment

Ranked in the UK's top 10 in the 2017 Complete University Guide, Aston Pharmacy excellent links with the profession. In addition, our research profile ensures relevant, expertise-led teaching for the students who enrol onto our courses each year. We have a long history of proving sector-leading courses - did you know that Aston Pharmacy School can trace its roots back to 1841?

You will learn in lectures, seminars, workshops and tutorials. Some modules may also use computer modelling and simulation sessions.

Our courses are assessed by a mixture of coursework, examinations, practical work and oral and written presentations. The research project module will be assessed on the basis of a submitted project report and an oral defence of a poster.

Your future career prospects

Graduates from our MSc programmes have taken up careers within the Pharmaceutical Industry in various disciplines such as analytical sciences, formulation development and project management. Our programmes provide the wider context and practical laboratory experience for pursuing careers in regulatory affairs, scientific writing and further studies.

Recent graduates have entered roles such as:
-Assistant Lecturer, University of Sulaimaniyah
-Associate Product Manager, AstraZeneca
-Business Development Manager, Crete Designs Limited
-Clinical Technician / Worker, Bridgewater Hospital
-Compound Technician, Sterling Pharmaceuticals
-Drug Designer, Unspecified Drug Company
-Drug Safety Specialist, PPD
-Drug Store Manager, Qaiwan group company
-Inhalation R & D Analyst, Aesica Pharmaceuticals Ltd (R5)
-Lecturer, University of Lagos, Nigeria
-Locum Pharmacist, various
-Molecular Modeller / Community Pharmacist, Verax Care Pharmacy
-OSD Technologist, GSK
-Pharma Benefit Associate, UnitedHealth Group
-Pharmacist, Government of India
-Pharmacist, Kerbala University
-Pharmacologist, Unspecified
-PhD Research Scholar, NIRMA University
-Recruitment Consultant, SRG
-Regulatory affairs trainee, PharmaLeaf India Pvt Ltd
-Research assistant, University of Leeds
-Research Scientist, Pluss Polymers
-Research Scientist, Wintean
-Researcher, Sunny Pharmtech Inc.
-Sales Relationship Coordinator, Wesley Assurance Society
-Science Teacher, Perry Beeches School
-Senior Regulatory officer, Roche Pharmaceuticals

Read less
This course is one of our three specialist pharmacy MSc courses (Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics). Read more
This course is one of our three specialist pharmacy MSc courses (Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics).

You’ll gain a thorough understanding and awareness of your chosen area of pharmacy, the research methods required to complete a final supervised research project and an overview of the drug discovery process.

These courses are primarily designed to prepare you for an academic or industrial career in the relevant area. You may be a scientist already working within the pharmaceutical industry or a recent science graduate.

You will undertake a variety of compulsory modules and a research project. This project will last approximately four months and you will work under the supervision of recognised experts in their field. The project allows you to undertake a detailed investigation and develop practical expertise in a specialist pharmaceutical sciences area. The University also has strong links with numerous pharmaceutical companies - there may be the opportunity to undertake your project in collaboration with one of these companies.

You will gain an overview of the drug development process from concept to market, gaining hands-on experience of pharmaceutical formulation and drug delivery.

What you will study

All students studying one of our three pharmacy MSc courses will take the following core modules:
-Research Methods 1: Professional Development
-Research Methods 2: Communication Skills
-Research Project
-Drug Discovery

Depending upon the course you chose, you will also undertake the following modules:
-Chemotherapy & Selective Toxicity
-Drug Dosage Form & Design
-Principles of Product Analysis and Validation
-Drug Delivery and Targeting

Learning, teaching & assessment

Ranked in the UK's top 10 in the 2017 Complete University Guide, Aston Pharmacy excellent links with the profession. In addition, our research profile ensures relevant, expertise-led teaching for the students who enrol onto our courses each year. We have a long history of proving sector-leading courses - did you know that Aston Pharmacy School can trace its roots back to 1841?

You will learn in lectures, seminars, workshops and tutorials. Some modules may also use computer modelling and simulation sessions.

Our courses are assessed by a mixture of coursework, examinations, practical work and oral and written presentations. The research project module will be assessed on the basis of a submitted project report and an oral defence of a poster.

Your future career prospects

Graduates from our MSc programmes have taken up careers within the Pharmaceutical Industry in various disciplines such as analytical sciences, formulation development and project management. Our programmes provide the wider context and practical laboratory experience for pursuing careers in regulatory affairs, scientific writing and further studies.

Recent graduates have entered roles such as:
-Assistant Lecturer, University of Sulaimaniyah
-Associate Product Manager, AstraZeneca
-Business Development Manager, Crete Designs Limited
-Clinical Technician / Worker, Bridgewater Hospital
-Compound Technician, Sterling Pharmaceuticals
-Drug Designer, Unspecified Drug Company
-Drug Safety Specialist, PPD
-Drug Store Manager, Qaiwan group company
-Inhalation R & D Analyst, Aesica Pharmaceuticals Ltd (R5)
-Lecturer, University of Lagos, Nigeria
-Locum Pharmacist, various
-Molecular Modeller / Community Pharmacist, Verax Care Pharmacy
-OSD Technologist, GSK
-Pharma Benefit Associate, UnitedHealth Group
-Pharmacist, Government of India
-Pharmacist, Kerbala University
-Pharmacologist, Unspecified
-PhD Research Scholar, NIRMA University
-Recruitment Consultant, SRG
-Regulatory affairs trainee, PharmaLeaf India Pvt Ltd
-Research assistant, University of Leeds
-Research Scientist, Pluss Polymers
-Research Scientist, Wintean
-Researcher, Sunny Pharmtech Inc.
-Sales Relationship Coordinator, Wesley Assurance Society
-Science Teacher, Perry Beeches School
-Senior Regulatory officer, Roche Pharmaceuticals

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DRUG INNOVATION. A UNIQUE PROGRAMME. The Dutch Master's Selection Guide (Keuzegids Masters 2017) ranked this programme as the best in the field of Chemistry in the Netherlands. . Read more

DRUG INNOVATION: A UNIQUE PROGRAMME

The Dutch Master's Selection Guide (Keuzegids Masters 2017) ranked this programme as the best in the field of Chemistry in the Netherlands. 

Drug Innovation is about:

  • developing new drugs to combat drug-resistant microorganisms
  • using gene or protein technologies to create therapies targeted at individual patients
  • finding a way to imprint the immune system to increase tolerance
  • exploring the relationship between gut microbes and brain disease
  • learning how to use proteomics to study stem cell development
  • reducing the side effects of treatment by finding new ways to deliver drugs directly onto the tumor
  • updating and speeding up the drug regulatory process

The Master’s in Drug Innovation programme focuses on diagnostics and the improvement and management of small molecule and biomolecular drugs. Drug innovation covers many topics such as the development of new vaccines and the study of antibodies, gene therapeutics, and medical nutrition. Once developed, a new drug then needs to go through approval, which raises a whole new set of challenges, for example the establishment of new methods and criteria for evaluating the quality, efficacy, safety, and performance of the drug.

INTERDISCIPLINARY PROGRAMME

This broad, interdisciplinary programme is open to graduates from a wide range of disciplines such as chemistry, biology, pharmaceutical sciences, biomedical sciences, or medicine.

MANY ELECTIVE COURSES

Our programme offers a diverse suite of elective courses. This means you can concentrate on the topics of most interest to you. You will also take an internship with one of the research teams working on drug innovation at Utrecht University. This work may lead to publication in scientific journals within the field or new drug patents or protocols.

Graduates of this programme may go on to undertake research in drug innovation at universities, in the pharmaceutical or and biotechnology industry or to work in science or healthcare.

PROGRAMME OBJECTIVE 

Programme

Drug innovation is an interdisciplinary field, which pulls together expertise from chemical, biological and medical sciences. This interdisciplinarity is central to the search for new solutions to currently incurable diseases. You will contribute to this field by undertaking two internships over a total of 15 months and submitting a writing assignment.

Graduated?

After graduation, you will have the skills needed to translate a drug-related problem into a relevant research question and will also be able to design and perform the research needed to solve this question. Finally, you will also be able to critically reflect on your own research and report on it, both verbally and in writing. These skills are highly transferable and will enable you to work independently within a competitive labour market.

TRACKS



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The Drug Development Science course is a highly flexible study programme designed for those working in or seeking to work in the field of clinical drug development. Read more

The Drug Development Science course is a highly flexible study programme designed for those working in or seeking to work in the field of clinical drug development. The course aims to provide students with expertise and skills in all aspects of clinical research, drug regulation and drug safety.

Key benefits

  • King's is ranked 7th in the world for Pharmacy & Pharmacology (QS World University Rankings by Subject 2017)
  • The study programme is compliant with both the PharmaTrain initiative of the European Commission and also with the Bologna Process.
  • Close links and regular speakers from pharmaceutical companies giving you insights and up-to-the-minute knowledge of drug discoveries.
  • Highly flexible programme with a part-time option that will allow you to study around your work schedule.
  • Delivered by leading experts from the academic staff of King’s College London, the biopharmaceutical sector and the regulatory authorities.

Description

The Drug Development Science programme offers you flexibility with the choice of modules and whether to study for a full masters qualification, a Postgraduate Certificate or Diploma. The MSc pathway is a one to four-year course that requires modules totalling 180 credits. The Postgraduate Diploma pathway can be studied over a period of two to three years and requires completed modules with a total of 120 credits. The Postgraduate Certificate route requires modules with a minimum total of 60 credits to achieve the award.

Course format and assessment

Teaching

We use lectures, seminars and group tutorials to deliver most of the modules on the course. You will also be expected to undertake a significant amount of independent study. There are 30 hours of lectures, seminars and workshops per module. Each module requires 2 to 4 hours of pre-reading and also exam preparation. 

For the MSc there are approximately 80 hours of tutorials, plus supervision of dissertation research and ad hoc academic tutor meetings. Students could spend 200 to 300 hours researching and writing a dissertation. 

Typically, one credit equates to 10 hours of work

Assessment

You will be assessed through a combination of coursework, practical assessments and examinations.

The study time and assessment methods detailed above are typical and give you a good indication of what to expect.

Career prospects

 It is expected that students who complete this course will be able to work in the clinical research arena at a higher level and this will open up job opportunities that might have previously been beyond their reach and enhance their value to their employers.

Sign up for more information. Email now

Have a question about applying to King’s? Email now



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Unique in Europe, this course combines biomedicine and pharmaceutical science to prepare you for a rewarding career in the pharmaceutical, bioscience or healthcare sectors. Read more
Unique in Europe, this course combines biomedicine and pharmaceutical science to prepare you for a rewarding career in the pharmaceutical, bioscience or healthcare sectors.

If you're interested in a career in the fascinating and challenging world of drug design, this is the course that will take you there.

Rather than presenting just one of the disciplines used in the field, this postgraduate degree, unique in Europe, blends the subjects you need - biomedicine and pharmaceutical science - into one comprehensive course that focuses on the integration of modern organomedicinal chemistry and molecular biology.

You’ll study various steps involved in developing and creating effective drugs, from concept to clinic, including the theories and practical applications of chemical drug design and immunology, pharmacology and molecular biology. Learning will be based on emergent technology from academic research and how it is applied to the drug development process, identification of drug targets, and development of effective drugs via reference to the relevant biological systems and pathways.

See the website http://www.napier.ac.uk/en/Courses/MSc-Drug-Design-and-Biomedical-Science-Postgraduate-FullTime

What you'll learn

This course provides the knowledge, understanding and practical experience you’ll need to forge a rewarding career in research and development in the pharmaceutical, bioscience or healthcare sectors. You’ll develop in-depth understanding of disease processes and molecular targets and an ability to apply this knowledge and theory to key aspects of drug design and biomedical science.

Equipped with the ability to follow developments in the field, you’ll learn to apply them to your work and make innovative contributions to the industry that will benefit others. Complex issues often arise in this field: you’ll acquire the skills necessary to make informed judgements and effectively communicate decisions.

There is an emphasis on developing your practical laboratory skills with various opportunities for hands-on experience in a range of current techniques and practices. In your final trimester you’ll undertake an independent project within a vibrant biomedical or drug design research team, allowing you to apply and further develop your technical, research and professional skills. There may be the opportunity to conduct your research project externally in a relevant organisation or industry in the UK or overseas.

You’ll also develop key skills including communication, problem solving, team work, project management, and leadership. You’ll learn through interactive lectures, workshops, tutorials, site visits and laboratory sessions, and by engaging with guided independent study. A variety of assessment tools are used to enhance and evaluate your learning.

This programme is also available as a Masters by Research: http://www.napier.ac.uk/research-and-innovation/research-degrees/courses

Modules

• Current practice in drug development
• Advanced immunology
• Molecular pharmacology and toxicology
• Research skills
• Quality Control and Pharmaceutical Analysis or Biotechnology and Drug Discovery
• Drug design and chemotherapy
• Research project

Study modules mentioned above are indicative only. Some changes may occur between now and the time that you study.

Careers

The rapidly developing pharmaceutical, bioscience and healthcare sectors all need qualified drug discovery or biomedical scientists. This course is your fastest and most effective route to a successful career in drug design.

You could establish a laboratory-based career with global pharmaceutical companies, developing biotechnology companies, contract drug testing, hospitals, NHS, local government or health and safety divisions.

Alternatively, further studies to PhD level are available at institutions all over the world leading to an academic career.

How to apply

http://www.napier.ac.uk/study-with-us/postgraduate/how-to-apply

SAAS Funding

Nothing should get in the way of furthering your education. Student Awards Agency Scotland (SAAS) awards funding for postgraduate courses, and could provide the help you need to continue your studies. Find out more: http://www.napier.ac.uk/study-with-us/postgraduate/fees-and-funding/saas-funded-courses

Read less
This course is one of our three specialist pharmacy MSc courses (MSc in Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics). Read more
This course is one of our three specialist pharmacy MSc courses (MSc in Pharmaceutical Sciences, Drug Delivery, or Pharmacokinetics).

You’ll gain a thorough understanding and awareness of your chosen area of pharmacy, the research methods required to complete a final supervised research project and an overview of the drug discovery process.

These courses are primarily designed to prepare you for an academic or industrial career in the relevant area. You may be a scientist already working within the pharmaceutical industry or a recent science graduate.

You will undertake a variety of compulsory modules and a research project. This project will last approximately four months and you will work under the supervision of recognised experts in their field. The project allows you to undertake a detailed investigation and develop practical expertise in a specialist pharmaceutical sciences area. The University also has strong links with numerous pharmaceutical companies - there may be the opportunity to undertake your project in collaboration with one of these companies.

During this course, you will gain the skills and knowledge required as a pharmacist - the ability to provide effective pharmaceutical formulation strategies for current and future drug therapies and medicinal products.

What you will study

All students studying one of our three pharmacy MSc courses will take the following core modules:
-Research Methods 1: Professional Development
-Research Methods 2: Communication Skill
-Research Project
-Drug Discovery

Depending upon the course you chose, you will also undertake the following modules:
-Chemotherapy & Selective Toxicity
-Drug Dosage Form & Design
-Principles of Product Analysis and Validation
-Pharmacology

Learning, teaching & assessment

Ranked in the UK's top 10 in the 2017 Complete University Guide, Aston Pharmacy excellent links with the profession. In addition, our research profile ensures relevant, expertise-led teaching for the students who enrol onto our courses each year. We have a long history of proving sector-leading courses - did you know that Aston Pharmacy School can trace its roots back to 1841?

You will learn in lectures, seminars, workshops and tutorials. Some modules may also use computer modelling and simulation sessions.

Our courses are assessed by a mixture of coursework, examinations, practical work and oral and written presentations. The research project module will be assessed on the basis of a submitted project report and an oral defence of a poster.

Your future career prospects

Graduates from our MSc programmes have taken up careers within the Pharmaceutical Industry in various disciplines such as analytical sciences, formulation development and project management. Our programmes provide the wider context and practical laboratory experience for pursuing careers in regulatory affairs, scientific writing and further studies.

Recent graduates have entered roles such as:
-Assistant Lecturer, University of Sulaimaniyah
-Associate Product Manager, AstraZeneca
-Business Development Manager, Crete Designs Limited
-Clinical Technician / Worker, Bridgewater Hospital
-Compound Technician, Sterling Pharmaceuticals
-Drug Designer, Unspecified Drug Company
-Drug Safety Specialist, PPD
-Drug Store Manager, Qaiwan group company
-Inhalation R & D Analyst, Aesica Pharmaceuticals Ltd (R5)
-Lecturer, University of Lagos, Nigeria
-Locum Pharmacist, various
-Molecular Modeller / Community Pharmacist, Verax Care Pharmacy
-OSD Technologist, GSK
-Pharma Benefit Associate, UnitedHealth Group
-Pharmacist, Government of India
-Pharmacist, Kerbala University
-Pharmacologist, Unspecified
-PhD Research Scholar, NIRMA University
-Recruitment Consultant, SRG
-Regulatory affairs trainee, PharmaLeaf India Pvt Ltd
-Research assistant, University of Leeds
-Research Scientist, Pluss Polymers
-Research Scientist, Wintean
-Researcher, Sunny Pharmtech Inc.
-Sales Relationship Coordinator, Wesley Assurance Society
-Science Teacher, Perry Beeches School
-Senior Regulatory officer, Roche Pharmaceuticals

Read less
The Clinical Pharmacology course will give you the advanced skills and knowledge to evaluate the safety of new medicinal products in preparation for medical approval. Read more

The Clinical Pharmacology course will give you the advanced skills and knowledge to evaluate the safety of new medicinal products in preparation for medical approval. It is one of three modular programmes in Pharmaceutical Medicine designed for working physicians, clinical scientists and allied health professionals interested in the clinical development process.

Key benefits

  • King's is ranked 7th in the world for Pharmacy & Pharmacology (QS World University Rankings by Subject 2017)
  • Lectures delivered by experienced multi-disciplinary researchers from the biopharmaceutical sector and the regulatory authorities.
  • Flexible study schedule with the option to complete a PG Diploma (coursework only) or PG Certificate.
  • Coordinated study programme with the PharmaTrain and the Faculty of Pharmaceutical Medicine of the Royal College of Physicians curricula.
  • The first UK course that complies with both the PharmaTrain initiative of the European Commission and the Bologna Process, and is the PharmaTrain Centre of Excellence.

Description

Clinical Pharmacology is the study of how drugs influence human physiology and the way the body responds. This study forms a vital part of the clinical development of new medicines and requires an advanced understanding of pre-clinical science, as well as the ethical and legal requirements for specialist research programmes. A well-designed clinical pharmacology programme informs the final regulatory of a new medicine. Therefore, generating skilled clinical pharmacologists is critical for the efficiency of future drug development.

This course will provide you with a broad knowledge and understanding of the drug development process and the medical aspects of the marketing of pharmaceutical products. You will also have opportunities to undertake advanced research projects and the possibility of one or more thesis publications.

The study programme is made up of optional and required modules. The MSc pathway requires modules totalling 180 credits to complete the programme, including 60 credits from a dissertation of around 15,000 - 18,000 words. The Postgraduate Diploma pathway will require modules totalling 120 credits, while the Postgraduate Certificate will require you to study modules totalling of 60 credits to complete the course.

If you are studying full-time, you will complete the course in one year, from September to September. If you are studying for the MSc qualification part-time, your programme will take up to four years to complete. The Postgraduate Diploma and Certificate pathways are both part-time courses. The Postgraduate Diploma will take two to three years to complete and the Postgraduate Certificate up to two years.

Course purpose

This course is for those working in or seeking to work in the field of clinical drug development. It covers all aspects of the clinical development process through from the earliest studies to post marketing activities. It will enhance knowledge and skills in all aspects of clinical research, drug regulation and drug safety.

Assessment

The primary method of assessment for this course is a combination of coursework and written examinations. The MSc study programme also requires a research and dissertation on the subject of clinical pharmacology.

The study time and assessment methods detailed above are typical and give you a good indication of what to expect. However, they are subject to change.

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IN BRIEF. Train for a career in the newly emerging industries of the post-genomic eraWork at the interface between biology and chemistryExcellent career prospectsPart-time study optionInternational students can apply. Read more

IN BRIEF:

  • Train for a career in the newly emerging industries of the post-genomic eraWork at the interface between biology and chemistryExcellent career prospectsPart-time study optionInternational students can apply

COURSE SUMMARY

Following completion of the Human Genome Project, the pharmaceutical industry is preparing for a revolution in cancer and inherited disorder therapies. This course is training a new generation of bioscientists to meet challenges at the interface between biology and chemistry, and to apply pharmaceutical and analytical knowledge directly to improve quality of life.

The course develops a broad knowledge and conceptual base in the field of drug design and discovery, with an emphasis on new developments and advances in drug identification, understanding drug pharmacology and novel therapeutics, and appreciating how these topics interact with bioscience businesses and enterprise.

This programme is designed to enable you to gain systematic knowledge and critical awareness of current problems and new insights regarding the analysis of biomolecules. There is particular reference to drug design and discovery, along with a comprehensive and critical understanding of applied techniques and their current application in research in the field of biomolecule analysis and drug design.

This course is aimed at students who wish to acquire the specialised skills needed to design drugs for the 21st century. It is ideal for anyone with primarily either a chemistry or biochemistry based undergraduate degree wishing to broaden their knowledge base. The part-time route is well suited to those who already work in industry as it is possible to carry out research projects within the place of work. Prospective students must be committed to developing their skills and knowledge for a career in the pharmaceutical or biotechnology sectors.

TEACHING

Teaching is through:

  • Lectures to provide thorough grounding in the techniques of biomolecule characterisation and drug design.
  • Practical sessions and workshops to demonstrate techniques and methods used in biomolecule characterisation and drug design, and provide a structured opportunity for you to practice techniques and methods in analytical biosciences and drug design.
  • Guided reading that will recommend texts, key articles and other materials in advance of, or following, lecture classes.  
  • The research project which will enable you to practice the application of appropriate, and selected, bioscientific techniques in an academic or industrial context, and demonstrate research methodologies and skills appropriate to and valuable with biomolecule characterisation and drug design. During your research project You will be supervised by expert staff who are actively engaged in international research programmes.

ASSESSMENT

There are eight taught 15 credit modules each of which have only one assessment (100%). Each exam is 2 hours.

EMPLOYABILITY

Although particularly relevant to those looking for a career in the pharmaceutical and biotechnology industries, this course will also equip you for a career in research, teaching and many other professions including cosmetic science, animal health, food science, medical laboratory research, patent law, scientific journalism and health and safety.

LINKS WITH INDUSTRY

Research projects may be carried out at other institutions (recently Universities in Bremen or France and the Paterson Institute, UK). We also invite visiting lecturers to share their expertise on the subject areas.

FURTHER STUDY

After completion of this course you may wish to specialise in a chosen subject area in one of the School’s two main research centres: Ecosystems and Environment Research Centre (EER) or Biomedical Research Centre (BRC).



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This course offers knowledge and expertise relevant to a senior role in clinical research in a pharmaceutical, biotechnology, device, contract research or site management company or the NHS. Read more

This course offers knowledge and expertise relevant to a senior role in clinical research in a pharmaceutical, biotechnology, device, contract research or site management company or the NHS.

Overview

If your line of work involves clinical research, this course is designed to help you advance and enhance your career.

Whether you work in the pharmaceutical industry, health service, for a contract research organisation, regulatory authority, data management organisation or in medical writing, we have tailored this programme to give you an outstanding grounding in clinical research skills and knowledge.

It’s the leading part-time, face-to-face MSc in Clinical Research and, by undertaking this course, you’ll be equipped to meet good clinical practice and regulatory quality standards for developing new healthcare interventions to improve treatments for patients.

The programme presents an overview of clinical trial processes and the regulations for bringing in a new chemical entity, and explores a broad range of therapeutic areas and their treatments in relation to clinical trials, drug registrations and drug safety.

We will support you to move confidently between these therapeutic areas and therefore increase your potential value to employers. In your dissertation year, you’ll be encouraged to carry out projects which have direct value to your employer, making this a highly attractive course for your employer to support.

This part-time MSc programme is recognised by the pharmaceutical industry and the Health Service as being of outstanding quality and practical value in the work place to clinical research professionals.

The programme is run over three calendar years of part-time study and is in a modular format. Teaching happens over four two-day sessions per year which takes place within Cardiff’s School of Pharmacy and Pharmaceutical Sciences. These session are always scheduled at weekends to accommodate students’ existing employment commitments.

Distinctive features

  • You will gain advanced understanding of best practice in clinical research to apply to running clinical trials.
  • You’ll experience in-depth training in drug development, clinical trials, and regulatory GCP requirement for clinical trials
  • Lecturers from Pharmaceutical Industry will provide you with an up-to-date overview on key developments in Clinical Research
  • Clinical Research trainers deliver a variety of teaching methods that enhance the course and will stimulate your learning.
  • The therapeutic modules will widen your skills in an array of medical settings.
  • The diversity of employment backgrounds of participants affords an ideal environment for networking with other clinical research personnel.
  • You’ll have the opportunity to undertake a research project at an internationally recognised research school at Cardiff University.
  • You’ll receive close academic support from an experienced personal tutor with an international background in compliance with clinical trial GCP and regulatory requirements.
  • You’ll develop critical analysis, personal reflection and enhanced clinical trial project communication and problem solving skills for career development in clinical research.

Career prospects

Clinical research is an expanding and highly competitive area. Undertaking this MSc will provide you with the skills and knowledge needed to advance and enhance a career in clinical research. 

This programme is suitable for graduates from healthcare, life sciences or other related disciplines, and healthcare professionals who are interested in a career in clinical trials in the health service, pharmaceutical, biotechnology, device industries, Contract Research Organisations/ suppliers to the pharmaceutical industry. It is also ideal for professionals working in clinical trials who wish to further develop their knowledge and skills of clinical trials.

Potential career opportunities include clinical trials, clinical research, clinical data management, regulation of clinical trials, medical writing, academic clinical trials, Phase I clinical trials units, the pharmaceutical industry, hospitals, archiving in clinical trials, quality assurance in clinical trials, clinical research project management, clinical trial administration, clinical trial co-ordinator, clinical trial administration/support to clinical trials and more.

After successfully completing this course, you will have an advanced standing both clinically and academically, with the potential to be at the forefront of your chosen profession.



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This Masters in Medicine course is offered to medical graduates in training who wish to develop their research skills, broaden their research interests, and develop advanced knowledge in selected areas of clinical and scientific practice. Read more
This Masters in Medicine course is offered to medical graduates in training who wish to develop their research skills, broaden their research interests, and develop advanced knowledge in selected areas of clinical and scientific practice. The course syllabus and curriculum have been developed following consultation with medical trainees in Ireland in order to ensure that the course fulfills their needs in terms of higher medical training at national and international level. The aim of the course is to provide advanced training in key domains of excellence relevant to modern medical practice for all students while also providing specialist knowledge relevant to their individual chosen career pathways.

Students will be required to complete twelve taught modules (5 ECTS each) as follows:

Six core modules (in year 1):

Professional and Ethical Practice of Medicine,
Research Skills I,
Research Skills II,
Health Services Management,
Health Informatics,
Patient Safety for Clinical Specialists.

Six optional modules (year 2) from either Molecular and Translational Medicine (strand A):

Cellular Biology and Cell signalling Mechanisms,
Introduction to Genetics and Molecular Biology,
Molecular oncology,
Molecular Mechanisms of Human disease I and II, and
laboratory skills for clinical specialists

or Population Health and Health Implementation (Strand B):

Public Health for Clinical Specialists,
Global Health for Clinical Specialists,
Rehabilitation Medicine for Clinical Specialists,
Teaching and Learning for Clinical Specialists,
Pharmacoeconomics, Pharmacoepidemiology, and Drug Safety 56

Students will also be required to submit a dissertation (30 ECTS) based on an original research/ laboratory-based project at the end of the second year.

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This course is designed for Scientists and Engineers who wish to develop their skills in drug analysis and toxicology. The course will enhance your career prospects and give you the confidence and competence to make a difference in this fascinating field. Read more

This course is designed for Scientists and Engineers who wish to develop their skills in drug analysis and toxicology. The course will enhance your career prospects and give you the confidence and competence to make a difference in this fascinating field.

You will benefit from the use of modern analytical equipment, and a real insight into the latest developments and challenges facing the industry. Your coursework will be underpinned by research, and industry-input, providing you with the best platform from which to deliver relevant and up-to-date analytical science services as a well-prepared graduate.

85% of MSc Analytical Sciences graduates have gone on to employment in analytical sciences and 12% have continued to PhD study (Business Gateway, 2017).

What you will study

SEMESTER 1

This course has a common first semester with the Analytical Science courses with other specialisms (Environmental Analysis, and Food Analysis, Authenticity and Safety).

However, the extensive laboratory module is tailored to emphasise analytical techniques most relevant to your chosen specialism of Drug Analysis and Toxicology.

SEMESTER 2

You will take part in a group problem-solving mini-project within your discipline. This builds on semester one study and emphasises the groups' ability to correctly apply appropriate instrumental techniques and methodology to solve the analytical problem posed. 

Control of Substances Hazardous to Health (COSHH), Ethics and Project Planning are introduced to the group and will provide you with valuable experience for your individual MSc Research Project Preparation which is carried out in the final 2-3 weeks of semester 2. 

The project titles are released at the beginning of semester two but not allocated until week 3 or 4. Allocation is often based on a competitive basis.

SEMESTER 3

You will begin the MSc Research Project practical work where you will develop your skills in using initiative, innovation, interpersonal skills, and a high level of autonomy, critical judgement and the application of appropriate and relevant principles in order to produce your thesis.

Teaching and assessment

A built-for-purpose learning environment fully supports your learning experience in analytical science. You are given extensive use of state-of-the-art analytical equipment, e.g. GC-MS, LC-MS, LC-MS-MS, ICP-AES, SEM-EDXA, CE, DSC, TGA, PCR, NMR and tuition from research active, expert staff. Much focus is placed upon developing you to work autonomously and problem-solve in analytical environments.

Our partners commonly provide industrial visits and guest lectures as well as external MSc projects. These relationships will allow you to gain a unique insight into the opportunities available within the analytical chemistry sector, as well as the challenges and opportunities you will face once in the workforce.

ACTIVITY SUMMARY

  • Lectures - 20 students per group, 10 hours per week
  • Seminars - 20 students per group, 1 hours per week
  • Webinar - 20 students per group, # hours per week
  • Tutorial - 20 students per group, 2 hours per week
  • Project Supervision - 20 students per group, 5 hours per week
  • Demonstration - 20 students per group
  • Practical class or workshop - 20 students per group, 1 hour per week
  • Supervised time in studio / workshop - 20 students per group
  • Field Work - 20 students per group
  • External Visits - students per group, 1 hour per week
  • Placement / Work Based Learning - 20 students per group

INDEPENDENT STUDY

You will develop substantial initiative and autonomy through lectures, tutorials and laboratory exercises which will demand a significant amount of independent learning to complete coursework and assessments. The MSc project is a significant piece of self-directed work which tests your higher cognitive skills in problem-solving and analysis, synthesis, evaluation and selectivity and improves your ability to learn.

STAFF DELIVERING ON THIS COURSE

Our team features in the annual Support and Teaching staff with Appreciation and Recognition (STAR) awards voted by the students and organised by RGU:Union. 

Most of our staff members are research-active or have connections to industry. Professional involvement in the design of this course ensures its alignment with the requirements of the industry and increases your employability. Our school has a unique relationships with, for example, Aberdeen's environmental industries, Scottish Food and Drink producers and the Medicines and Healthcare Regulatory Agency (MHRA). We also collaborate with the Scottish Police Authority on the profile analysis of seized and surrendered abused drugs.

ASSESSMENT

Typically students are assessed each year:

  • 1 written exam typically for 2.5 hours
  • 3 written assignments, including essays
  • 1 report
  • 1 dissertation
  • 14 set exercises
  • 4 oral assessments
  • 1 practical skills assessment

Placements

Depending upon availability and academic performance, you may have the opportunity to undertake your MSc Research Project in an industrial setting. This may be in the Aberdeen area or further afield, e.g. other parts of Scotland, Switzerland, Spain, Belgium, France etc. We have a dedicated Placement Office to support you to securing a placement, however most students achieve placement from their own independent networking. Please note that industry projects are limited and subject to availability.

Job prospects 

85% of MSc Analytical Sciences graduates have gone on to employment in analytical sciences and 12% have continued to PhD study (Business Gateway, 2017).

Graduates gain employment in a wide range of areas such as research, project management and analytical services associated with a range of industries including distillation, pharmaceutical, oilfield chemistry, food/drink analysis and environmental science.

Graduates may also go on to further their academic career by seeking doctoral studies either within Robert Gordon University, when funding and suitable vacancies are available, or the rest of the UK, EU or internationally.

Some of our graduates with the Drug Analysis and Toxicology specialism have gone on to undertake a variety of projects including tablet quality analysis at GSK, substances of abuse analysis for Police Scotland, and toxicology analysis at Aberdeen Royal Infirmary Hospital.

How to Apply

Please visit the website to find out how to apply



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Our Youth Justice, Community Safety and Applied Criminology Masters fills a two-fold gap in current academic provision. It provides experienced practitioners with the opportunity to apply academic knowledge to, and critically analyse and assess, the context in which they work. Read more
Our Youth Justice, Community Safety and Applied Criminology Masters fills a two-fold gap in current academic provision. It provides experienced practitioners with the opportunity to apply academic knowledge to, and critically analyse and assess, the context in which they work.

If you have a limited knowledge of criminal justice, the course offers a detailed understanding of the agencies in the criminal justice system, their functions and responsibilities. You can take up to a third of the course as an internship within a criminal justice agency.

The flexibility of the course also allows you to complete up to a third of the course through work based learning.

We expand your awareness of the social and political context of working with offenders.In-depth analysis includes 'what works' and the concept of risk assessment; key criminological theories including cultures of punishment; the legal and organisational context of crime; mediation and reparation schemes; victims and victimology; community safety; mental health issues; the history and development of youth justice; the problem of youth and youth as a problem; and drug misuse and drug-related crime.

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Accelerated training for the Biopharmaceutical Industry. Application deadline. 17th June 2018. This unique professional training programme has been designed and developed in collaboration with the multinational Contract Research Organisation, . Read more

Accelerated training for the Biopharmaceutical Industry

Application deadline: 17th June 2018

This unique professional training programme has been designed and developed in collaboration with the multinational Contract Research Organisation, Covance.

The course is 20 months long, covering campus-based taught modules in the first six months, followed by a 12-month guaranteed paid placement in industry where you can expect to earn around £20,000.

During your training you’ll gain an integrated understanding of the full biological drug development pathway and the regulatory framework. The focus will be on large molecule drugs: monoclonal antibodies like Herceptin, bio-similars and antibody-drug conjugates; gene therapies and the technologies that underpin the discovery and development pathway.

You’ll be taught by leading industrialists and internationally renowned academics working at the forefront of their fields in the areas of science that support drug development. The curriculum is delivered primarily via project work in teams, and is assessed with outputs that are commonplace in industry, including presentations and reports to clients, regulators, investors/sponsors etc.

To prepare you for work in industry, you’ll also have access to cutting-edge practical technologies and gain hands-on practical training in protein purification, characterisation, formulation and assessment of binding function. In addition, you’ll use cell-based assays to look at drug potency, all performed in a strict regulated environment.

This course will help give you the experience and skills to become highly employable. Many pharmaceutical companies are expanding their biopharmaceutical capability, which is creating demand and opportunities for talented, well-trained people. At the same time, these companies report difficulties in recruiting employees with relevant skill sets and those with broad industrial experience are greatly sought after.

Course content

This course will provide you with an understanding of biological drug development focusing on each of the major steps of the process:

  • discovery
  • manufacturing
  • pre-clinical testing
  • clinical trials
  • market access and
  • the regulatory and legal aspects framework that ensure safe practice and the development of safe and effective medicines.

Course structure

The course is 20 months long, covering the campus-based taught elements in six to seven months, followed by a 12-month guaranteed paid work placement involving a research project where you’ll experience at first hand the working environment of this industry.

Work placement: an integral part of your training

An integral part of this course is your first paid job in industry. This is a 12-month guaranteed work and research experience in industry or placement hosted within the university research laboratories developed and co-supervised with industry. Students can expect to earn up to £20,000 over the duration of their placement.

The placements will all include a practical research project where you will gain in-depth practical experience of at least one technical function of the drug development process (discovery, manufacturing, pre-clinical testing, clinical safety and efficacy).

You will commence your project in May, six-months after the start of the programme and will be completed by the following April. Graduation is scheduled immediately thereafter, making you available for employment immediately after your placement.

These are typical modules/components studied and may change from time to time. Read more in our Terms and conditions.

Year 1

Over the first six to seven months starting in September you will study 100 credits worth of taught modules.

Compulsory modules:

  • Biopharmaceutical Development Pathway 5 credits
  • Biopharmaceutical Drug Discovery and Pre-Clinical Testing 20 credits
  • Manufacturing Biopharmaceuticals 20 credits
  • Integrated Drug Development Plan 10 credits
  • Biopharmaceutical Development: Clinical 10 credits
  • Commercialising Biopharmaceutical Products 10 credits
  • Practical Skills for a Regulatory Environment 25 credits

Year 2

Seven months after the start of the course (April/May), you will start a 12-month industrial placement where you will undertake a research project worth 80 credits.

Compulsory modules:

  • Industrial Placement & Research Project 80 credits

For more information on typical modules, read Biopharmaceutical Development MSc in the course catalogue

Learning and teaching

The learning and teaching on the course has been constructed to align with activities performed in industry, preparing you to be work-ready immediately after you finish.

You’ll have access to the very best learning resources and academic support during your studies. We’ve been awarded a Gold rating in the Teaching Excellence Framework (TEF, 2017), demonstrating our commitment to delivering consistently outstanding teaching, learning and outcomes for our students.

This course will challenge you to think creatively, solve problems and develop strong communication and teamwork skills. You’ll experience a wide range of teaching methods, including formal lectures, interactive workshops, practical classes and industry site visits.

You’ll extensively use of real-life, industry specific case studies to illustrate theoretical and practical concepts and multiple opportunities to work in teams, including the opportunity to lead a team. A wide range of ‘authentic’ assessments will be used that students will experience in the workplace including submissions to regulatory authorities, client reports and presentations to industry panel members.

Career opportunities

Your first steps into an industrial career

The course is designed to train talented scientists wishing to pursue a career in drug development in the international biopharmaceutical industry.

You’ll be exposed to senior industrialists working as tutors throughout the course and can take this opportunity to obtain career advice. You’ll also work in industry full time for 12 months, which is an outstanding opportunity for you to develop a competitive career plan.

With this degree, you’ll have the relevant knowledge and experience to fast-track your career as, for example, an analytical scientist, project manager, or coordinator, in areas such as research, quality control, manufacturing, project management, non-clinical, clinical, and market access.

As a student on this course you’ll have unique access to an industry-mentor and a personal tutor (academic member of staff) for the duration of your studies. You’ll also get support in planning your career through sessions that develop your CVs and applications.



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