Clinical Research Associate
Job Description:
Job Responsibilities:
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Site monitoring, source verification, query resolution & ensuring protocol compliance
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Visit investigator sites for initiation, monitoring & close-out activities
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Support eTMF, CTMS, EDC documentation and trial coordination
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Track patient recruitment, AE/SAE reporting, IP accountability, and site communications
Required Qualification:
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B.Pharm / M.Pharm / MSc Clinical Research / Life Sciences
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1–3 years CRA experience in CRO or clinical trial setting (oncology, metabolic, FIH preferred but not mandatory)
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Knowledge of ICH-GCP, regulatory requirements & monitoring practices
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Willingness to travel for monitoring visits
Company Profile
Our client is a tested & trusted name in Indian pharmaceutical industry having more than 35 years of experience in manufacturing and exporting of pharmaceutical formulations, trading of raw materials and Research & Development for pharmaceutical Industry. Dedicated to providing the best quality products in pharmaceutical, biotechnology & healthcare Industry, our client is at paramount & has a strong presence in exports, generic formulations, ethical range of products, institutional & government supplies as well as recognized as Government approved R & D facility by Department of Science and Technology, Government of India.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.