This role involves overseeing biospecimen management in 5-12 clinical trials with minimal supervision, developing Specimen Management Plans, and providing biospecimen input in protocol authoring
Job Summary
This role involves overseeing biospecimen management in 5-12 clinical trials with minimal supervision, developing Specimen Management Plans, and providing biospecimen input in protocol authoring.
Responsibilities include tracking and reconciling biospecimen status, ensuring vendor documents align with protocol, and providing regular biospecimen status updates to the core clinical team.
Bristol Myers Squibb offers a supportive culture, opportunities for growth, and competitive benefits, emphasizing balance and flexibility in the work environment.
Matching Summary
This role involves overseeing biospecimen management in 5-12 clinical trials with minimal supervision, developing Specimen Management Plans, and providing biospecimen input in protocol authoring.