BSc Hons Accounting and Management
Queen Mary University of London's BSc-Hons- Accounting and Management program ...
Charterhouse Square
INTAKE: September
The MSc in Clinical Drug Development program at Queen Mary University provides students with a deep understanding of the multifaceted process of bringing new drugs from concept to market.
Pharmacology and Drug Discovery: Students gain insights into the principles of pharmacology, drug interactions, and mechanisms of action, laying the foundation for understanding drug development.
Clinical Trial Design: The curriculum delves into the intricacies of designing and conducting clinical trials, including phases, protocols, patient recruitment, and ethical considerations.
Regulatory Guidelines: Students explore the regulatory framework governing drug development, including approvals, compliance, and safety monitoring set by international agencies.
Data Analysis and Interpretation: The program equips students with skills to analyze and interpret clinical trial data, ensuring accurate assessment of drug efficacy and safety.
Ethical and Legal Aspects: Students examine ethical dilemmas, patient consent, and legal aspects surrounding drug development, ensuring adherence to ethical standards.
Drug Safety and Pharmacovigilance: The curriculum covers post-marketing surveillance, adverse event reporting, and strategies for ensuring patient safety post-approval.
Health Economics and Market Access: Students explore the economic considerations of drug development, pricing, and strategies for achieving market access and reimbursement.
Collaboration and Partnerships: The program emphasizes the importance of collaborations between academia, industry, and regulatory bodies in driving successful drug development.
Quality Assurance and Good Clinical Practice: Students learn about quality assurance measures and good clinical practice standards to ensure the reliability of trial results.
Drug Development Lifecycle: The curriculum provides a holistic view of the drug development lifecycle, from pre-clinical research to post-marketing surveillance.
Research Project: Students undertake a research project, allowing them to apply their knowledge and skills to address real-world challenges in clinical drug development.
Charterhouse Square
IELTS 6.5
£ 26750
Postgraduate Entry Requirements:
Students must provide:
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.
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.