Clinical Trial Management The City University of New York

Overview

The Clinical Trial Management programme at The City University of New York is designed to equip students with the advanced scientific and regulatory expertise required to lead complex medical research projects. This comprehensive Master of Science curriculum focuses on the operational, ethical, and data-driven aspects of modern drug and device development.

Students engage with a curriculum that bridges the gap between laboratory science and clinical application. The course structure is tailored to accommodate working professionals, offering evening and weekend sessions alongside asynchronous online learning. This flexibility ensures that individuals currently active in the biotech or pharmaceutical sectors can advance their qualifications without interrupting their careers.

Why Clinical Trial Management at The City University of New York?

The university provides a distinctive learning environment that integrates academic excellence with industry-relevant training. Students benefit from a curriculum developed by the Department of Biology, which emphasises real-world application through a required internship that can be completed in various locations, including out-of-state placements.

The programme offers significant enrichment opportunities, including participation in campus-wide seminars and regional scientific conferences. These platforms allow students to present research and network with established professionals. The institution's strong links to the New York metropolitan pharmaceutical hub provide a strategic advantage for those seeking to influence the future of healthcare.

Tuition Fee Breakdown

• International fee: USD 855 per credit
• National fee: USD 855 per credit
• Local fee: USD 470 per credit

Visit the Fees and Funding section for a breakdown in your local currency.

Syllabus

The curriculum consists of 30 core credits and 6 elective credits. Modules may include:

• Clinical Research and Clinical Trial Terminology
• Regulatory Affairs in a Global Environment
• Clinical Trial Project Management
• Advanced Biostatistics
• Ethical Consideration for Clinical Research
• Clinical Trial Implementation
• Medical Writing--Document preparation
• Clinical Trial Data Management
• Drug Safety and Pharmacovigilance
• Clinical Trial Management Capstone Project
• Clinical Epidemiology
• Global Regulatory Affairs
• Medical Writing: Document Submission
• Medical Writing: Investigational Applications for Drugs, Biologics and Medical Devices
• Medical Writing: Drugs, Biologics and Medical Devices License Applications
• Clinical Trial Quality and Compliance
• SAS Programing
• Advanced Pharmacology
• Advanced Toxicology
• International Regulatory Affairs

Careers with Clinical Trial Management

Graduates are prepared for a diverse range of high-level roles within the pharmaceutical, biotechnology, and medical device industries. The programme's focus on regulatory science and project management opens doors to careers as clinical investigators, research administrators, and regulatory affairs managers.

Additional career pathways include roles as clinical data managers, quality assurance consultants, and drug safety specialists. Many alumni find success within major medical centres, contract research organisations, and government health agencies, where they oversee the development of life-saving vaccines and therapeutic treatments.