Clinical Trial Associate, Clinical Operations
Bristol-Myers SquibbFull Time
Junior (1 to 2 years), Mid-level (3 to 4 years)
Candidates should possess a Graduate or Bachelor's degree in life sciences or a related field. Experience with clinical trial coordination, study setup, maintenance, and archival is expected. Familiarity with clinical study regulations, procedures, policies, and guidelines is necessary. Experience in vendor management, CRO oversight, and country oversight is also required.
The Clinical Trial Coordinator – Project Specialist will partner with the Study Manager on end-to-end operational study delivery, focusing on internal systems, databases, and project plans. They will work cross-functionally with internal and external partners on clinical study management activities, supervise study conduct and progress, and identify/resolve risks. Responsibilities include reviewing key clinical documents, developing study plans, facilitating interactions with internal and external partners, managing vendors and CROs, overseeing country-specific activities, coordinating study-related communications, supervising the delivery of clinical supplies, ensuring data oversight and eTMF completeness for inspection readiness, and managing study budgets including Task/Change Orders and expenses.
Provides life sciences products and services
Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.