About the role
Position DetailsRole: Clinical Research CoordinatorLocation: DelhiEmployment Type: Full-timeExperience: 2-4 Years
Key Responsibilities
- Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
- Support study start-up activities and assist with site initiation.
- Participate in recruitment and retention of study subjects.
- Complete and maintain source documents, CRFs, and logs accurately.
- Compile and update the Site Master File.
- Manage Investigational Products (IP), including accountability and shipping.
- Coordinate submissions and communication with the Ethics Committee.
- Update sponsors on study progress and prepare for monitoring visits.
- Perform other responsibilities assigned by management.
Who Can Apply
- Freshers with a completed Clinical Research course.
- Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.
- Strong interest in clinical trials and regulatory compliance.
- Excellent organizational, communication, and documentation skills.
Why Join Us?🌟 Gain hands-on experience in clinical trials.🌟 Learn directly from experienced professionals.🌟 Be part of innovative projects that shape the future of healthcare.🌟 A great opportunity to grow your career in clinical research.