Contract, Clinical Operations
Axsome Therapeutics IncFull Time
Senior (5 to 8 years), Expert & Leadership (9+ years)
Candidates must possess a Graduate/Bachelor's degree in life sciences or a related field, coupled with at least 1+ year of relevant work experience in a pharmaceutical or scientific environment. Foundational knowledge of clinical study delivery processes, including regulations and industry standards, is essential, as are strong project management skills and excellent verbal and written English communication. Proficiency in Microsoft Office tools and clinical trial management systems is also required.
The Clinical Trial Coordinator will collaborate with the Study Manager or Study Delivery Lead on end-to-end operational study delivery activities, from setup to archival. Responsibilities include ensuring the completeness of internal systems, collaborating with internal and external partners, monitoring study conduct, resolving risks and issues, reviewing key clinical documents, and developing study plans. The role also involves facilitating communication, coordinating vendor relationships and study-specific deliverables, managing country-specific activities and budgets, overseeing clinical supply delivery, ensuring inspection readiness with eTMF oversight, and managing budget aspects including Task/Change Orders and expense tracking.
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.