- Conduct site monitoring visits to ensure compliance with regulatory requirements, study protocols, and company standards.
- Collaborate with investigators, sponsors, and CROs to resolve issues related to clinical trials.
- Prepare reports on study findings, including adverse events (AEs), serious adverse events (SAEs), and other relevant data.
- Ensure timely submission of documents such as case report forms (CRFs) and query resolution letters.
Job Requirements :
- 3-5 years of experience in clinical research or a related field.
- Solid understanding of ICH-GCP guidelines and regulations governing clinical trials.
- Excellent communication skills for effective collaboration with cross-functional teams.
📌 Clinical Research Associate (Mumbai)
🏢 SUN PHARMA
📍 Mumbai
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