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Sr. Manager, Biospecimen Management

5-6 years
Not Disclosed
10 Nov. 28, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Manager, Biospecimen Management

Location: Hyderabad, Telangana, India
Job Type: Full-Time
Category: Clinical Research / Laboratory Management


About Bristol Myers Squibb (BMS)

At Bristol Myers Squibb, we deliver life-changing innovations that transform the lives of patients worldwide. From cutting-edge cell therapies to advanced clinical trials, our teams tackle challenging scientific problems with purpose and precision. Working at BMS means being part of a high-achieving, collaborative environment where your contributions directly impact patient outcomes and your career growth is supported through diverse learning opportunities.

Learn more: careers.bms.com


Position Overview

BMS is seeking a Senior Manager, Biospecimen Management to lead and oversee biospecimen operations for Phase 1–4 clinical trials and externally sourced biospecimens. This role is responsible for developing, implementing, and managing protocol-specific biospecimen strategies, ensuring timely specimen handling, tracking, and reporting. The ideal candidate is a strategic thinker, capable of solving complex operational challenges, managing vendor relationships, and supporting cross-functional teams to optimize biospecimen workflows.

This role requires 5–6 years of experience in academic, biotech, pharmaceutical, or healthcare industries, with hands-on knowledge of biospecimen lifecycle management, clinical trial operations, and regulatory compliance.


Key Responsibilities

  • Biospecimen Lifecycle Management: Oversee collection, storage, tracking, utilization, and final disposition of biospecimens for clinical studies.

  • Strategy & Planning: Lead development of Specimen Management Plans, operationalize study-specific strategies, and manage critical timelines to support clinical decision-making.

  • Vendor & Stakeholder Management: Coordinate with central labs, bioanalytical vendors, CROs, and storage facilities. Resolve operational issues and track inventory with minimal supervision.

  • Data & Reporting: Maintain biospecimen trackers using Excel, Spotfire, Tableau, or Polaris; prepare management reports and ensure compliance with study protocols.

  • Quality & Risk Management: Identify and mitigate biospecimen-related risks, manage Critical-to-Quality (C2Q) processes, and maintain protocol compliance.

  • Cross-Functional Collaboration: Actively participate in clinical team meetings, mentor junior staff, and serve as a subject matter expert on biospecimen management.

  • Innovation & Process Improvement: Develop innovative solutions to streamline operations and enhance efficiency across clinical teams.


Required Qualifications

  • Education: Scientific degree (Associate, Bachelor’s, Master’s, or higher) or equivalent project management experience.

  • Experience:

    • 5–6 years in biospecimen management, clinical research, or related laboratory operations.

    • Experience with clinical trial operations, vendor management, and regulatory compliance (GCP, GLP, CLIA).

    • Demonstrated expertise in managing biospecimen lifecycle, data flows, and reporting processes.

  • Skills:

    • Strong analytical and problem-solving abilities.

    • Excellent communication and stakeholder management skills.

    • Ability to operate independently, prioritize tasks, and manage multiple projects simultaneously.

    • Proficient in Excel, Tableau, Spotfire, or similar data tracking tools.

    • Knowledge of drug discovery and development processes preferred.


Work Environment & Travel

  • Work Setting: Primarily Hyderabad, with on-site presence required as per study team needs.

  • Travel: Minimal (0–5%) to support site training or vendor due diligence.


Why Join BMS

At BMS, you’ll be part of a mission-driven culture focused on “Transforming patients’ lives through science™.” We value diversity, inclusion, and work-life balance while offering opportunities to take on challenging, meaningful work in a collaborative global environment.

Benefits include:

  • Comprehensive health and wellness programs

  • Competitive remuneration and annual performance-based bonus

  • Professional development opportunities and mentorship programs

  • Supportive and inclusive work environment

BMS encourages applications from candidates with diverse backgrounds and experiences. Qualified candidates with arrest or conviction records will also be considered in accordance with local laws.


Apply Today: Advance your career with BMS and contribute to life-changing therapies that impact patients worldwide.