Are you a nursing professional or life sciences graduate looking to advance your career in clinical research? Auriga Research, a leading Contract Research Organization (CRO), is hiring a Clinical Research Coordinator (CRC) in Delhi NCR. If you have a passion for clinical trials, GCP compliance, and patient-centric research, this could be your perfect opportunity!
📋 Job Description: Clinical Research Coordinator (CRC)
As a CRC, you will play a crucial role in managing clinical trials, ensuring protocol adherence, and maintaining regulatory compliance. Your responsibilities will include:
✔ Assisting in clinical trial execution as per ICH-GCP guidelines.
✔ Coordinating with investigators, ethics committees, and sponsors for smooth trial operations.
✔ Managing subject recruitment, consent, and follow-up visits.
✔ Maintaining accurate trial documentation (ICFs, CRFs, source documents).
✔ Ensuring timely data entry, query resolution, and sample dispatch.
✔ Supporting monitoring visits, audits, and regulatory inspections.
✅ Eligibility Criteria
- B.Sc./M.Sc. in Nursing, Life Sciences, or related field.
- 2–3 years of experience in clinical trials (preferred).
- Strong understanding of ICH-GCP & clinical research processes.
- Excellent communication & organizational skills.
- Ability to multitask & work in a fast-paced environment.
🏢 About Auriga Research Pvt. Ltd.
Auriga Research is a leading CRO in India, specializing in clinical trials, bioequivalence studies, and regulatory services. With a commitment to quality and compliance, Auriga partners with global pharmaceutical companies to deliver reliable and ethical research solutions.
📩 How to Apply?
If you meet the qualifications and are excited about this CRC role in Delhi NCR, send your updated CV to:
📧 Email: snehendu@aurigaresearch.com
