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Clinical Research Associate (Cra) I/Ii

1-3 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

Clinical Research Associate (CRA) I/II

Company: IQVIA
Industry: Clinical Research / Pharmaceuticals
Job Type: Full-time


Position Details:

Job Title: Clinical Research Associate - I/II
Job Location: Any Metro City


Qualifications & Experience:

  • Education Required:

    • B.Pharm / M.Pharm

    • Pharm D / BHMS / BAMS / BDS

  • Experience: 1-3 years of onsite monitoring experience is a must.

    • Note: Freshers will not be considered for this role.


Job Overview & Responsibilities:

  • Perform monitoring and site management work to ensure that clinical trial sites comply with study protocols, regulatory guidelines, and sponsor requirements.

  • Conduct site monitoring visits (including selection, initiation, monitoring, and close-out visits).

  • Ensure that study data is accurately collected, reported, and documented according to Good Clinical Practice (GCP) standards.


Application Process:

📩 Interested candidates can share their resume at:
🔹 ashwini.veerabhadrappa@iqvia.com