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Clinical Trial Support Specialist / Clinical Trial Specialist

2-4 years
Not Disclosed
10 Dec. 6, 2024
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 Opening: Clinical Trial Support Specialist / Clinical Trial Specialist

Company: Bristol Myers Squibb
Location: Hyderabad (Hybrid, 2–3 days onsite per week)
Experience Required: 2 to 4 years


Key Responsibilities

  • Strong expertise with CTMS, Veeva Vault, and project management.
  • Hands-on experience with:
    • Data entry in tools.
    • Document uploads.
    • Quality control (QC) processes.
    • Clinical Study Report (CSR) preparation.
    • Reconciliation of CTMS/eTMF.
  • Comprehensive knowledge of ICH GCP guidelines.
  • Ability to understand various trial types and working models.
  • Proficient in MS Office, especially Excel.
  • Effective communication skills.

Preferred Background

  • Experience with CROs or small biotech companies is highly desirable.

How to Apply

If you meet the criteria and are passionate about advancing your career in clinical trials, we encourage you to apply.

Send your updated resume to:
pooja.shree@iqvia.com