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Clinical Research Associate @ Clariwellglobal

Home > Pharmacist / Medical Representative

 Clinical Research Associate

Job Description

     

    • Assist in planning, initiation, monitoring, and completion of clinical trials.

    • Conduct site qualification, initiation, routine monitoring, and close-out visits.

    • Ensure all trial activities are conducted according to protocol, SOPs, GCP, and applicable regulatory guidelines.

    • Verify that clinical data is accurate, complete, and verifiable from source documents.

    • Maintain essential documents and track trial progress in the Trial Master File (TMF).

    • Support communication between sponsors, investigators, and site staff.

    • Identify and resolve issues that arise during study conduct.

    • Ensure subject safety and proper reporting of adverse events (AEs/SAEs).

    • Prepare visit reports and follow-up letters as per timelines.

    • Participate in investigator meetings and training sessions.

     

Employement Category:

Employement Type: Full time
Industry: Pharma / Biotech
Role Category: Pharmacist / Medical Representative
Functional Area: Not Specified
Role/Responsibilies: Clinical Research Associate

Contact Details:

Company: Clariwellglobal
Location(s): Bengaluru

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Keyskills:   regulatory affairs medical coding pharma clinical research pharmacovigilance

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Clariwellglobal

We are Clinical Research service provider company based in Pune. We offer Site Management & Clinical Trial services across India. Currently we have clientele in Pune, Mumbai, Banglore, Ahmedabad, Hyderabad and Chennai.