Back
Tier-1 pharma brand and metro location increase interest, but specialized biospecimen skills limit applicant pool.
Role relies on specialized clinical biospecimen and vendor experience, limiting cross-industry transferability.
Requires explicit 3+ years plus specific biospecimen, vendor, and regulatory experience and training.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Manage biospecimen oversight for 5-12 BMS-sponsored Phase 1-4 clinical trials, including developing and implementing specimen management plans with risk mitigation.
Provide regular status updates on biospecimen inventory, location, quality, and timelines to core clinical teams; act as liaison between clinical teams and vendors resolving issues independently.
Support audit readiness, participate in vendor audits and cross-functional process optimizations, and provide training and mentorship to colleagues.
Scientific degree (Associates, Bachelors, Masters, or higher) with project management or equivalent experience.
3+ years of experience in academic, biotech, healthcare, or pharmaceutical industry related to biospecimen management.
Intermediate knowledge of clinical biospecimen procedures, vendor management, and applicable regulations (GCP, GLP, CLIA).
Travel: minimal, 0%-5% as required by organization.
Experienced managing multiple clinical trials' biospecimen logistics and compliance from Phase 1 through 4 with ability to prioritize and resolve complex issues independently.
Operationally focused, capable of providing regular, actionable updates to cross-functional clinical teams and driving process improvements.
Able to mentor colleagues and drive change agility while maintaining audit-ready documentation in a regulated environment.