Global healthcare and life sciences leader IQVIA has announced recruitment for the position of Clinical Research Coordinator (CRC) across Noida, Kochi, and Thane locations in India. The company is seeking professionals with 6 months to 3 years of experience in clinical research who are passionate about advancing healthcare through clinical trials.
This is an excellent opportunity for candidates looking for Clinical Research Coordinator jobs in India, especially those aiming to build their careers with a globally recognized clinical research organization.
Job Overview
| Particulars | Details |
|---|---|
| Organization | IQVIA |
| Position | Clinical Research Coordinator (CRC) |
| Locations | Noida, Uttar Pradesh; Kochi, Kerala; Thane, Maharashtra |
| Experience | 6 Months – 3 Years |
| Employment Type | Full-time / Fixed Term Contract |
| Preferred Candidates | Immediate Joiners |
| Industry | Clinical Research, Healthcare, Life Sciences |
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences and healthcare industry. The company supports pharmaceutical, biotechnology, and medical device organizations by delivering innovative solutions that accelerate clinical development and improve patient outcomes worldwide.
Key Responsibilities of Clinical Research Coordinator
Selected candidates will be responsible for:
- Coordinating day-to-day clinical trial activities at study sites.
- Managing study documentation and maintaining regulatory files.
- Assisting investigators in patient recruitment and scheduling study visits.
- Ensuring compliance with Good Clinical Practice (GCP) and ICH guidelines.
- Coordinating communication between investigators, sponsors, and clinical teams.
- Maintaining accurate clinical trial records and essential documents.
- Supporting data collection, reporting, and site management activities.
- Tracking study timelines and ensuring protocol adherence.
Eligibility Criteria
Candidates applying for the IQVIA Clinical Research Coordinator position should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related healthcare disciplines.
- Experience ranging from 6 months to 3 years in clinical research.
- Good understanding of clinical trials, research documentation, and GCP guidelines.
- Excellent organizational and coordination abilities.
- Strong communication and interpersonal skills.
- High attention to detail and problem-solving capabilities.
Preferred Skills
- Knowledge of ICH-GCP guidelines
- Clinical trial documentation management
- Site coordination and monitoring support
- Time management and multitasking abilities
- Proficiency in MS Office applications
- Ability to work in a collaborative environment
Salary and Benefits
Estimated Salary: ₹3.0 – ₹6.5 LPA (depending on qualifications and experience)
Why Join IQVIA?
- Opportunity to work with a global leader in healthcare and life sciences.
- Exposure to large-scale clinical research projects.
- Excellent learning and career advancement opportunities.
- Dynamic and collaborative work environment.
- Hands-on experience in clinical trials and patient-centric research initiatives.
How to Apply
Interested and eligible candidates can send their updated CV to:
Email: ajaykumar.s@iqvia.com
Candidates who can join immediately are encouraged to apply at the earliest.