Are you passionate about clinical research and oncology? Do you want to contribute to groundbreaking cancer research while working at one of India’s most prestigious hospitals? TATA MEMORIAL HOSPITAL, Mumbai, is hiring a Clinical Trial Coordinator for its Oncology Unit. This is a fantastic opportunity to gain hands-on experience in clinical trials, collaborate with top oncologists, and make a meaningful impact in the field of oncology research.
Location: TATA MEMORIAL HOSPITAL, Mumbai
Timings: 9:00 AM – 6:00 PM
Compensation: ₹20,000 per month
Duration: 6-month role (with potential for extension)
Apply Now: Send your resume to hr@jarurat.care, srijan@jarurat.care, or ahsan@jarurat.care
Key Responsibilities
As a Clinical Trial Coordinator, you will play a crucial role in the successful execution of oncology trials. Your responsibilities will include:
🔹 Assisting Oncologists: Support oncologists in clinical trial activities and patient coordination.
🔹 Documentation: Maintain case report forms (eCRFs), trial logs, and regulatory documents.
🔹 Compliance: Ensure adherence to ICH-GCP, NDCT Rules, and ICMR Guidelines.
🔹 Liaison Role: Act as a bridge between investigators, sponsors, and ethics committees.
🔹 Adverse Event Reporting: Monitor and report adverse events (AE/SAE) as per regulatory requirements.
Who Should Apply?
Education:
✔ Bachelor’s Degree: B.Pharm, B.Sc in Life Sciences, Biotechnology, or related fields (Mandatory).
✔ Master’s Degree: M.Pharm, M.Sc in Clinical Research, Oncology, or related fields (Preferred).
✔ Certifications: Additional certifications in clinical research, biostatistics, or oncology trials will be advantageous.
Experience:
✔ Minimum 6 months of experience in clinical research, oncology trials, or data coordination.
✔ Hands-on experience with Informed Consent Forms (ICF), AE/SAE reporting, and protocol compliance.
✔ Familiarity with FDA, CDSCO, and EMA regulations is a plus.
Skills Required:
✔ Communication: Strong verbal and written communication skills for effective collaboration.
✔ Attention to Detail: Precision in data entry and regulatory documentation.
✔ Technical Proficiency: Proficiency in Microsoft Office, statistical tools, and research databases.
How to Apply
If you’re ready to take the next step in your clinical research career, we encourage you to apply!
Send your resume to:
✉ hr@jarurat.care
✉ srijan@jarurat.care
✉ ahsan@jarurat.care
