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Trial Supplies Manager

1-2 years
Not Disclosed
10 May 1, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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: Trial Supplies Manager

Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb
Employment Type: Full-time
Industry: Pharmaceuticals / Clinical Supply Chain
Posting Date: April 2025


Position Summary

Bristol Myers Squibb is seeking a Trial Supplies Manager to develop and manage global clinical supply strategies for investigational products. The role ensures on-time delivery and regulatory compliance of clinical supplies in collaboration with internal teams and external vendors, supporting BMS’s mission of transforming patients’ lives through science.


Key Responsibilities

  • Develop and maintain global supply strategies for clinical studies.

  • Collaborate with internal (e.g., Drug Development, PDQ) and external partners to align supply with study and regulatory needs.

  • Forecast, monitor, and analyze clinical supply demand versus usage.

  • Issue manufacturing and packaging/labeling requests and support global distribution.

  • Review IRT specs and manage depot/site distribution plans.

  • Maintain compliance with import/export regulations and monitor use-date extension.

  • Act as primary contact for supply issues, change controls, and inspection readiness activities.

  • Contribute to cross-functional meetings and vendor coordination.

  • Support budgeting through forecasting and cost tracking.

  • Lead or participate in writing SOPs and departmental process documents.


Qualifications

  • Bachelor’s degree in Science, IT, or Business (focus on IT, Supply Chain, or digitization preferred).

  • Minimum 2 years of pharma industry experience; 1+ year in global clinical supply or development.

  • Knowledge of clinical trial supply chain, forecasting, labeling, and logistics.

  • Strong project management, communication, and negotiation skills.

  • Familiarity with IVRS, CTMS, import/export regulations, and eTMF systems.

  • Demonstrated ability to manage cross-functional teams and drive consensus.


Work Model

  • Site-by-design role; hybrid with at least 50% onsite work expected.


Benefits

  • Competitive compensation and benefits.

  • Inclusive culture focused on innovation, flexibility, and personal growth.

  • Opportunities to contribute to life-changing therapies.