BSc (Econ)(Hons) Economics, Finance and Management
Spanning three years, with options to extend to four or five years to include a year ab...
MSc Clinical Drug Development
Charterhouse Square
INTAKE: September
Program Overview
This program provides a comprehensive understanding of the clinical drug development process, from preclinical testing to post-market surveillance. It focuses on the regulatory, clinical, and operational aspects of drug development, ensuring that students are well-prepared for the challenges of bringing new medications from the laboratory to the clinic. The program is ideal for those seeking careers in the pharmaceutical industry, clinical research organizations, or regulatory bodies.
Curriculum: The MSc curriculum is designed to provide both depth and breadth in clinical drug development. Core modules cover topics such as pharmacology, drug safety, clinical trial design, regulatory affairs, and biostatistics. Students are also introduced to topics like the ethical considerations in drug development, clinical data management, and the application of biotechnology in drug discovery. The program includes practical training in the form of workshops and case studies, allowing students to develop problem-solving skills. A significant feature of the program is the research project or dissertation, where students undertake independent research in a specific area of clinical drug development.
Research Focus: The research focus of the MSc in Clinical Drug Development is on bridging the gap between laboratory research and clinical practice. Students engage with cutting-edge research in areas such as clinical pharmacology, drug toxicity, personalized medicine, and regulatory science. The program encourages students to explore the latest developments in clinical trials and how new therapeutic agents are evaluated for safety and efficacy. Students also have the opportunity to collaborate with research teams working on drug development projects, fostering an environment that encourages scientific inquiry and innovation.
Industry Engagement: Queen Mary University of London has strong connections with the pharmaceutical industry, clinical research organizations, and regulatory agencies. These relationships provide students with access to industry professionals, guest lectures, and opportunities for internships or placements in leading pharmaceutical companies. The program also facilitates networking events where students can meet potential employers and gain insights into the latest industry trends. Industry collaboration ensures that students receive a practical, real-world education that is directly aligned with current industry practices.
Global Perspective: With a diverse student body and faculty, the MSc in Clinical Drug Development at Queen Mary University of London adopts a global perspective. The program incorporates international case studies, allowing students to explore drug development processes in different regulatory environments and health systems. This global outlook helps students understand the challenges and opportunities in drug development across different markets, preparing them to work in an increasingly interconnected global pharmaceutical industry.
Location
Charterhouse Square
Score
IELTS 6.5
Tuition Fee
£ 29950
Postgraduate Entry Requirements:
- Applicants should have successfully completed a bachelor's degree or its equivalent from a recognized institution with a minimum overall score of 60% or equivalent.
- English language proficiency is required, and applicants must provide evidence of their English language skills through an approved language test.
- IELTS: A minimum overall score of 6.5 with no individual component below 6.0.
- TOEFL: A minimum overall score of 92, with at least with at least 17 in Listening, 18 in Reading, 20 in Speaking, and 21 in Writing.
- PTE Academic: A minimum overall score of 71 with 65 in Writing, and 59 in Reading, Listening and Speaking..
- Some postgraduate programs may have specific subject prerequisites or additional requirements.
Students must provide:
- academic marksheets & transcripts
- letters of recommendation
- a personal statement - SOP
- passport
- other supporting documents as required by the university.
Work experience: Some postgraduate courses may require relevant work experience in the field.
It is important to note that meeting the minimum entry requirements does not guarantee admission, as the university considers factors such as availability of places and competition for the program. Additionally, some courses may have higher entry requirements or additional selection criteria, such as interviews or portfolio submissions.
Queen Mary University of London offers a range of scholarships and bursaries to its students.
Queen Mary International Excellence Scholarships: A scholarship program for international undergraduate and postgraduate students who have an offer of admission from Queen Mary University of London and have demonstrated academic excellence. The scholarship covers full tuition fees for one year of study.
Queen Mary Law Scholarships: A scholarship program for undergraduate and postgraduate law students who have an offer of admission from Queen Mary University of London and have demonstrated academic excellence. The scholarship covers full or partial tuition fees, depending on the level of academic achievement.
Queen Mary Engineering and Materials Science Scholarships: A scholarship program for undergraduate and postgraduate students studying engineering or materials science who have an offer of admission from Queen Mary University of London and have demonstrated academic excellence. The scholarship covers full or partial tuition fees, depending on the level of academic achievement.
Graduates of the MSc in Clinical Drug Development program are well-equipped to pursue a variety of roles within the pharmaceutical and healthcare industries. This program opens doors to diverse career opportunities.
Clinical Research Associate: Graduates can work as CRAs, overseeing clinical trials, monitoring patient safety, and ensuring compliance with protocols and regulations.
Regulatory Affairs Specialist: Graduates may specialize in regulatory affairs, navigating the complex landscape of regulatory approvals and compliance.
Clinical Project Manager: Graduates can lead clinical trial teams, coordinating various aspects of trial execution, data collection, and reporting.
Medical Writer: Graduates may work as medical writers, crafting accurate and clear documentation for clinical trial protocols, reports, and regulatory submissions.
Pharmacovigilance Specialist: Graduates can contribute to drug safety by monitoring adverse events, analyzing data, and ensuring compliance with pharmacovigilance regulations.
Clinical Development Coordinator: Graduates can assist in the planning, execution, and management of clinical trials, collaborating with cross-functional teams.
Health Economics Analyst: Graduates may analyze economic data to inform pricing, reimbursement, and market access strategies for new drugs.
Regulatory Consultant: Graduates can offer consulting services to pharmaceutical companies, providing insights into regulatory compliance and strategy.
Clinical Trial Auditor: Graduates can ensure the quality and integrity of clinical trials by conducting audits and inspections of trial sites and processes.
Pharmaceutical Project Manager: Graduates may manage projects related to drug development, from pre-clinical research to post-market activities.
Academic Researcher: Graduates with a research focus may pursue doctoral studies (Ph.D.) in clinical research, contributing to academic advancements in drug development.
