About the Role 📝
As a CRA, you’ll play a key role in managing clinical trials, ensuring compliance with regulatory standards, and driving innovation in healthcare.
Key Responsibilities 📊
- Site Feasibility & Investigator Selection: Identify and finalize investigators, negotiate study budgets, and execute contracts.
- Ethics Committee (EC) Submissions: Prepare and submit study documents for EC approval.
- Clinical Trial Monitoring: Oversee site initiation, monitoring, and close-out activities.
- Investigator Training: Train site personnel on study protocols, GCP, and trial procedures.
- Patient Recruitment & Data Management: Ensure timely enrollment, data entry, and query resolution.
- Safety Reporting: Manage SAE and SUSAR reporting per regulatory and Sun Pharma PV policies.
Requirements 📚
- Education: Bachelor’s or Master’s in Biology, Chemistry, Nursing, Pharmacy, Public Health, or Post-Graduate Diploma in Clinical Research.
- Experience: 1-5 years in clinical research.
- Skills: Knowledge of GCP practices, regulatory guidelines, and site management expertise.
Why Join Sun Pharma? 🌈
- Growth Opportunities: Develop skills in clinical trials and regulatory compliance.
- Collaborative Environment: Work with experienced professionals and cross-functional teams.
- Innovative Culture: Contribute to cutting-edge clinical research and innovation.
How to Apply 📧
Apply now through the below Link 👇🏻:
https://www.linkedin.com/redir/redirect/?url=https%3A%2F%2Fcareers%2Esunpharma%2Ecom%2Fjob%2FMumbai-Clinical-Research-Associate-%2528Clinical-Trials%2529%2F48646544%2F&urlhash=j_UH&isSdui=true
About Sun Pharma 🌟
Sun Pharma is a global leader in specialty generics, with operations in over 100 countries and a commitment to improving patient lives.
