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Sr. Associate Biobank

Amgen
Amgen
3-5 years
₹12,00,000 – ₹18,00,000 per year
Hyderabad
10 March 11, 2026
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

Sr. Associate Biobank – Amgen (Hyderabad)

Amgen is hiring a Senior Associate Biobank in Hyderabad, India for its Research division. This role focuses on managing biospecimen storage, consent governance, and biobank operations related to clinical trials and biomedical research. The position involves ensuring that biospecimen samples are stored, tracked, and used in compliance with clinical research regulations, informed consent policies, and biobank governance standards. You will work closely with biobank program managers, research scientists, clinical operations teams, and study coordinators to manage biospecimen inventory, consent verification, and long-term sample storage processes. This role is ideal for professionals with experience in biospecimen management, biobank operations, clinical trial sample handling, and laboratory information management systems (LIMS). The estimated salary for this role ranges from ₹12 LPA to ₹18 LPA depending on experience in clinical research, biospecimen operations, and laboratory data management.

Key Responsibilities

  • Verify participant consent documentation including permissions for future research, pharmacogenetics, and biomarker studies.

  • Manage biospecimen sample selection according to study protocols and consent restrictions.

  • Oversee long-term biospecimen storage tracking and retention timelines.

  • Execute and document sample destruction or return workflows when required.

  • Generate “no backup” sample lists and initiate destruction work orders when necessary.

  • Coordinate long-term storage (LTS) conversion processes after study completion.

  • Maintain audit logs and documentation supporting consent decisions and sample disposition.

  • Ensure accurate reconciliation between physical biospecimen inventory and LIMS records.

  • Support biobank operations for future research programs and biomarker discovery initiatives.

Required Qualifications

  • Master’s degree with 3+ years of experience in clinical trials or biospecimen operations, OR

  • Bachelor’s degree with 5+ years of experience in clinical research or biobank management.

  • Prior experience in biospecimen handling, sample management, or biobank operations.

  • Strong understanding of clinical trial processes and research compliance standards.

Required Skills

  • Biospecimen Management

  • Biobank Operations

  • Laboratory Information Management Systems (LIMS)

  • Clinical Trial Sample Handling

  • GCP / GxP Compliance

  • Sample Storage & Cold Chain Management

  • Regulatory Documentation & Audit Support

  • Data Traceability & Inventory Reconciliation

Salary

Approximate Salary: ₹12,00,000 – ₹18,00,000 per year (depending on experience in biospecimen management and clinical research operations).