- Location
- Delhi
- Type
- Full-time
- Department
- Healthcare
- Experience
- 2+ years
- Source
- Keka
Description
About the Job
We are looking for passionate and detail-oriented Clinical Research Coordinators (CRCs) to join our growing team. This is an exciting opportunity for professionals with 2–4 years of experience in clinical research, or for those with a background in life sciences/pharmacy and a certification in clinical research, who aspire to build a strong career in clinical trials and research operations.
The CRC will play a key role in managing clinical study activities, ensuring protocol compliance, and maintaining high standards of documentation and data integrity.
Position Details
Role: Clinical Research Coordinator
Location: Delhi
Employment Type: Full-time
Experience: 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.
Skills
GCPClinical TrialsCompliance