HRAPL has announced an exciting opportunity for experienced Clinical Research Coordinators (CRC) across Nagpur, Nashik, and Wardha, Maharashtra. Candidates with 2–3 years of clinical trial site experience and a background in Life Sciences, Biotechnology, Pharmacy, or related disciplines are invited to apply.
This is an excellent opportunity for professionals looking to advance their career in clinical research, clinical trial coordination, and site management while working in a dynamic research environment. Immediate joiners will be given preference.
HRAPL Clinical Research Coordinator Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company | HRAPL |
| Position | Clinical Research Coordinator (CRC) |
| Job Type | Full-Time |
| Experience | 2–3 Years |
| Qualification | Graduate in Life Sciences, Biotechnology, Pharmacy or related fields |
| Locations | Nagpur, Nashik & Wardha, Maharashtra |
| Vacancies | 3 (1 position at each location) |
| Preference | Immediate Joiners |
| Application Mode |
Key Responsibilities
As a Clinical Research Coordinator, you will be responsible for:
- Coordinating day-to-day clinical trial site activities.
- Managing patient recruitment, scheduling, and follow-up visits.
- Handling informed consent (ICF) documentation accurately.
- Maintaining essential study documents and regulatory files.
- Ensuring compliance with study protocols and ICH-GCP guidelines.
- Coordinating with Principal Investigators, Clinical Research Associates (CRAs), sponsors, and site staff.
- Ensuring timely and accurate data documentation.
- Supporting clinical monitoring visits and audits.
- Maintaining high-quality clinical research operations.
Required Qualifications
Candidates should possess:
- Graduate degree in Life Sciences, Biotechnology, Pharmacy, or related disciplines.
- 2–3 years of experience in clinical trial site operations.
- Strong understanding of:
- Clinical trial coordination
- Patient management
- Informed Consent Form (ICF) process
- Essential document maintenance
- Working knowledge of:
- ICH-GCP Guidelines
- Study protocols
- Regulatory requirements
- Excellent communication and organizational skills.
Preferred Skills
- Strong attention to detail
- Patient coordination expertise
- Documentation accuracy
- Regulatory compliance knowledge
- Team collaboration
- Clinical operations management
- Ability to work with investigators and CRAs
Job Locations
HRAPL is hiring for:
- Nagpur
- Nashik
- Wardha
One vacancy is available at each location.
Why Join HRAPL?
Working as a Clinical Research Coordinator at HRAPL offers:
- Opportunity to work on clinical research projects.
- Exposure to regulated clinical trial environments.
- Professional growth in clinical operations.
- Collaborative work culture.
- Opportunity to work alongside experienced investigators and research professionals.
How to Apply
Interested candidates should send their updated resume to:
Email: contact@hrapl.in
