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Clinical Research Associate @ Triventure Services

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 Clinical Research Associate

Job Description

    • Perform site initiation, routine monitoring, and close-out visits.
    • Review and verify case report forms (CRFs) against source documents.
    • Identify and resolve data discrepancies.
    • Ensure proper documentation and timely reporting of adverse events.
    • Maintain effective communication with investigators, sponsors, and regulatory authorities.
    • Assist in the preparation of regulatory submissions and documentation.
    • Provide training and support to site staff as needed.
    • Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements.
    • Support the initiation, monitoring, and close-out of clinical trial sites under supervision.

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Allied Health Services
Functional Area: Not Specified
Role/Responsibilies: Clinical Research Associate

Contact Details:

Company: Clariwellglobal
Location(s): Pune

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Keyskills:   clinical data management pharmacovigilance clinical research

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₹ 0 to 2 Yr

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Triventure Services

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