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    Job · 22087668

    Bristol-Myers Squibb logo

    Associate Director, Consent, Biospecimens & Imaging - Hyderabad

    Bristol-Myers Squibb · Hyderabad · onsite · Posted 4d ago

    Not disclosed6–8 yrsfulltimeSourced fromFoundit

    About a minute. You'll make an account on the way through.

    About this role

    At Bristol Myers Squibb, our employees often ask, Who are you working for—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

    This position reports to the Executive Director, Head of Consent, Biospecimens & Imaging (CBI). As a Line Manager, you will be responsible for leading and developing team members within the Specimen Data & Systems, Imaging Management, and Informed Consent for Specimens & Data functions located in the BMS Hyderabad office. The role provides people leadership, operational oversight, strategic direction, and workforce planning to ensure the effective delivery of global clinical trial support across specimen systems, imaging operations, and informed consent management. The incumbent will foster a high-performing, collaborative environment while driving operational excellence, quality, compliance, innovation, and continuous improvement across all areas of responsibility.

    Position Responsibilities

    • Responsible for the line management of the Specimen Systems & Data, Imaging Management, and Informed Consent for Specimens & Data teams in Hyderabad
    • Perform side-by-side coaching, deliver performance evaluations and goal setting, and provide ongoing mentoring, talent development, hiring, onboarding, and training to foster a high-performing and engaged organization.
    • Partner with the Heads of Specimen Data & Systems, Imaging Management, and Informed Consent for Specimens & Data to prioritize work, establish goals, optimize resource allocation, and support the development and continuous improvement of processes, procedures, systems, and capabilities.
    • Ensure alignment with functional leaders regarding body-of-work distribution, resource planning, capacity management, and business priorities across the respective teams.
    • Develop a strong understanding of the functional responsibilities within scope and provide leadership, guidance, and escalation support for day-to-day operational activities.
    • Establish, monitor, and report organizational metrics, performance indicators, quality measures, and resource utilization to support operational excellence and continuous improvement.
    • Lead and contribute to integration efforts that facilitate seamless global operations, support follow-the-sun models, and drive process improvement and standardization initiatives across internal and external stakeholders.
    • Champion innovation, digital transformation, and continuous improvement initiatives that enhance the efficiency, quality, compliance, and scalability of CBI operations.
    • Contribute to CBI strategic objectives, operational initiatives, organizational development efforts, and cross-functional programs that advance the mission and goals of the organization.

    Key Competency & Experience Requirements

    • BA/BS or equivalent degree in relevant discipline.
    • Minimum preferred of 6 years of global experience in clinical drug development, biospecimen management or related experience
    • Minimum preferred 2 years of people management.
    • Deep understanding of the clinical trial process with particular focus on the end-to-end clinical biospecimen and/or imaging lifecycle, as well as understanding of informed consent for use of biospecimens and data.
    • Demonstrated experience supporting clinical trials within the biopharmaceutical, healthcare, laboratory, CRO, or related clinical research environment.
    • Demonstrated people leadership experience, including coaching, performance management, talent development, and building high-performing teams.
    • Strong stakeholder management skills with the ability to influence without authority, resolve conflicts, and successfully lead through change.
    • Proven ability to lead cross-functional initiatives and effectively coordinate activities across internal and external stakeholders.
    • Knowledge of vendor oversight and partnership management, including experience working with central laboratories, imaging vendors, CROs, biomarker laboratories, bioanalytical providers, and biorepository partners.
    • Ability to identify organizational challenges, drive process improvements, and implement scalable solutions that improve quality, efficiency, and business outcomes.
    • Strong decision-making, problem-solving, and risk-management capabilities with a focus on accountability, quality, and compliance.
    • Enterprise mindset with the ability to think strategically, navigate ambiguity, and balance local priorities with global business objectives.
    • Demonstrated leadership behaviors reflecting urgency, accountability, integrity, innovation, and a continuous improvement mindset.

    We hire for skills and capabilities, not just credentials – if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

    How We Work

    Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

    Supporting People With Disabilities

    BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [HIDDEN TEXT]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

    Candidate Rights

    BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

    For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

    Data Protection

    We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

    Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

    If this posting is missing required information required by local law or incorrect, contact BMS at [HIDDEN TEXT] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

    R1607676 : Associate Director, Consent, Biospecimens & Imaging - Hyderabad

    Sourced from foundit

    Skills

    People managementProblem SolvingDecision MakingProcess Improvementcross-functional initiativesVendor Oversightclinical drug developmentbiospecimen managementStakeholder Management

    About Bristol-Myers Squibb

    Bristol-Myers Squibb logo

    Bristol-Myers Squibb

    Pharma

    375

    employees

    1887

    139 years old

    New York

    United States

    ₹19.1L PA avg

    Avg at Bristol-Myers Squibb

    About

    We are a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. At Bristol Myers Squibb, we work every day to transform patients’ lives through science. We combine the agility of biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation. We have the brightest people in the industry and believe that their diverse experiences and perspectives help to bring out our best ideas, drive innovation and achieve transformative business results. Each day, our employees around the world work together for patients – patients are at the center of everything we do. They inspire us. They are the reason we come to work each day. We are proud of the advancements we have made in oncology, hematology, immunology, and cardiovascular disease, and we are dedicated to helping patients prevail over serious diseases through our diverse and promising pipeline and new scientific platforms. We are pursuing therapies at the forefront of scientific discovery with the goal of bringing an exciting new generation of life-changing treatments to patients. We aspire to be at the center of a vibrant healthcare innovation ecosystem, where academic research centers, biotech, and biopharma companies all contribute to continued scientific advancement.

    Industries

    PharmaBiotech & Life sciences

    Employee ratings

    10 reviews

    3.7/ 5

    Culture

    2.6

    Career growth

    2.2

    Work-life

    3.1

    Employees rate it well for

    Work-Life Balance38Compensation & Benefits37

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