Manager,BiospecimenManagement

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). · Oversee biospecimen management in 5-12 clinical trials, with minimal supervision · Develop Specimen Management Plan, highlighting risks and providing mitigations steps. · Provide biospecimen input in protocol authoring to ensure operational feasibility and regulatory compliance. · Track and reconcile biospecimen status using internal and external systems. · Enter biospecimen requirements into a contracting system and ensure vendor documents (e.g. lab manuals, lab specs) are aligned with protocol and sample management plan. · Provide regular biospecimen status updates to core clinical team (inventory, location, quality issues, timelines). · Adhere to standard operating procedures and guidance documents · Act as a liaison between clinical teams and vendors to coordinate biospecimen activities and resolve issues with minimal supervision. · Participate in vendor audits and assist with CAPA resolutions. · Maintain study documents in ‘inspection ready’ state. · Participate in cross-functional projects aimed at optimizing workfl