Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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