NEXVED RESEARCH has announced an exciting opportunity for experienced clinical research professionals to join as a Clinical Research Coordinator (CRC) in Chandigarh. Candidates with experience in clinical trial coordination, patient management, and ICH-GCP compliance are encouraged to apply for this site-based clinical research job.
This Clinical Research Coordinator job in Chandigarh is ideal for candidates looking to advance their careers in clinical operations, site management, and clinical trial execution within the pharmaceutical and healthcare research industry.
About NEXVED RESEARCH
NEXVED RESEARCH is actively hiring skilled Clinical Research Coordinators to support ongoing clinical trials and research operations at its Chandigarh study site. The organization focuses on maintaining regulatory compliance, patient safety, and quality-driven clinical research practices.
Clinical Research Coordinator (CRC) Job Responsibilities
The selected candidates will be responsible for managing and coordinating daily clinical trial activities at the site.
Key Responsibilities
- Coordinate day-to-day clinical trial activities at the study site
- Support Investigators and CRAs in study-related operations
- Ensure compliance with ICH-GCP guidelines and study protocols
- Maintain accurate clinical study documentation and site records
- Assist in patient recruitment, coordination, and follow-up activities
- Ensure timely reporting and regulatory documentation
- Collaborate with sponsors, monitors, and internal clinical teams
- Maintain data accuracy and audit readiness
Eligibility Criteria
Educational Qualification
Candidates should possess any of the following qualifications:
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Life Sciences
- Other relevant healthcare or clinical research-related degrees
Experience Required
- 1–3 years of Clinical Research Coordinator (CRC) experience preferred
- Experience in clinical trial site coordination and documentation management is advantageous
Skills Required
- Strong understanding of ICH-GCP guidelines
- Good communication and interpersonal skills
- Excellent organizational and documentation abilities
- Ability to manage multiple clinical trial activities efficiently
Why Apply for This CRC Job in Chandigarh?
- Opportunity to work in active clinical trials
- Exposure to clinical operations and regulatory processes
- Career growth in the clinical research industry
- Work closely with investigators, sponsors, and CRAs
- Strengthen expertise in patient coordination and trial management
How to Apply
Interested and eligible candidates can share their updated CV via email:
📩 Email: info.nexvedresearch@gmail.com
Applicants are advised to mention “Application for Clinical Research Coordinator – Chandigarh” in the email subject line for faster processing.