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Associate Director, Product Manager Clinical Data Ecosystem

15+ years
Not Disclosed
10 Feb. 24, 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

Job Title: Associate Director, Product Manager Clinical Data Ecosystem
Location: Hyderabad, TS, India
Company: Bristol Myers Squibb

Position Summary

Bristol Myers Squibb (BMS) is committed to transforming patients' lives through science. This role is part of the Global Drug Development (GDD) IT team, responsible for delivering platform, data, and analytics capabilities for GDD Global Biostatistics and Data Sciences, Clinical Data Management, and related areas.

Key Responsibilities

Product & Team Management

  • Define product strategy and roadmaps for Clinical Data Ecosystem.

  • Identify product scope, feature stories, value proposition, and success criteria.

  • Manage a team of ~10 IT professionals, including Data Engineers, Solution Architects, Product Analysts, UX Designers, and Scrum Masters.

  • Define schedules, budgets, and ensure timely delivery of technology solutions.

Stakeholder Collaboration

  • Partner with GDD, Global Biometric & Data Science (GBDS), and Enterprise Data and Analytics Platform teams to influence and shape technology strategies.

  • Act as a Subject Matter Expert (SME) in GDD Data & Analytics Solutions.

  • Evaluate GDD data enhancements and assess prioritization with onshore and vendor teams.

  • Provide guidance on Clinical Data Ecosystem trends, including AI/ML and GenAI applications in clinical trial execution.

Operational & Strategic Leadership

  • Lead the end-to-end implementation of data solutions.

  • Oversee project, enhancement, and break/fix efforts.

  • Ensure alignment with emerging industry trends and best practices.

  • Mentor team members to develop their full potential.

  • Optimize vendor service delivery and balance workload between in-house and vendor teams.

Governance & Compliance

  • Stay current with industry regulations and Good Clinical Practices (GCP).

  • Lead process improvement initiatives to enhance efficiency and compliance.

  • Drive adoption of agile and product-oriented approaches within teams.

Qualifications & Experience

Education & Experience

  • Bachelor's degree in Computer Science, Information Technology, Life Sciences, or related field (Advanced degree preferred).

  • 15+ years of experience in the pharmaceutical industry, with expertise in clinical data acquisition, trial execution, and analysis.

  • 5+ years of experience delivering niche technology products in clinical development (e.g., Retrospective Trial Design Intelligence, Digital Study Design, Clinical Data Warehouse, Auto Mapper, etc.).

Technical & Domain Expertise

  • Strong knowledge of clinical data standards (CDASH, SDTM, ADaM).

  • Experience working with AWS data services (Glue, Redshift, Athena, Lake Formation) and Tableau Labs is a plus.

  • Hands-on experience in cloud-based data solutions.

  • Knowledgeable in regulatory guidelines and industry best practices.

Leadership & Communication

  • Proven ability to manage diverse, geographically distributed teams.

  • Strong communication and stakeholder engagement skills.

  • Ability to drive process improvements and manage cross-functional teams.

  • Experience in agile and product-based environments.

Why You Should Apply

  • Be part of a diverse and innovative team making a real impact on patients’ lives.

  • Work in a dynamic environment with access to cutting-edge technology.

  • Competitive benefits, career growth opportunities, and flexible work arrangements.

Equal Opportunity Employer Statement

BMS is dedicated to ensuring that individuals with disabilities excel through a transparent recruitment process and reasonable workplace accommodations. Applicants can request accommodations before accepting a job offer. Visit careers.bms.com/eeo-accessibility for the complete Equal Employment Opportunity statement.

On-site Protocol

BMS offers diverse work arrangements:

  • Site-Essential: 100% onsite.

  • Site-by-Design: Hybrid (at least 50% onsite).

  • Remote-by-Design: Remote work with required travel for business needs.