HRAPL (Hector Research and Archival Pvt. Ltd.), a leading Site Management Organization (SMO) in India, is hiring a Clinical Research Coordinator (CRC) with 2-3 years of experience for its operations in Nagpur, Maharashtra.
This role offers a chance to contribute to high-quality clinical trial management in a precision-driven environment focused on excellence and regulatory compliance.
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About the Company
Hector Research and Archival Pvt. Ltd. (HRAPL) is India’s preferred Site Management Organization (SMO) specializing in comprehensive clinical trial services.
As an ISO 9001:2015 certified company headquartered in Nagpur, HRAPL provides end-to-end site management, including patient recruitment, enrollment, data management, trained resources (coordinators, nurses, pharmacists), project management, and multi-site support across clinics, general hospitals, and multi-specialty centers.
Committed to timelines, budget efficiency, and world-class standards, HRAPL partners with sponsors to advance clinical research in India through innovative approaches, ICH-GCP compliance, and a focus on quality and patient safety.
Job Details
- Company Name: Hector Research and Archival Pvt. Ltd. (HRAPL)
- Experience: 2 to 3 years in clinical trial site operations
- Qualification: Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields
- Location: Nagpur, Maharashtra
- Work Type: On-site
- Open Positions: 1
Job Description
HRAPL is seeking a dedicated Clinical Research Coordinator to manage daily clinical trial site activities in Nagpur. The role focuses on ensuring smooth operations, protocol adherence, and high-quality data collection in support of sponsor trials.
Clinical Research Coordinator
- Department: Clinical Research / Site Management
- Role: Site coordination, patient management, and documentation for clinical trials
- Experience: 2 to 3 years
- Education/Qualification: Graduate in Life Sciences / Biotechnology / Pharmacy or related
Skills / Qualifications
- Strong patient coordination and workflow management
- Proficiency in Informed Consent Form (ICF) handling and essential trial documentation
- Effective coordination with Principal Investigators, Clinical Research Associates (CRAs), and site teams
- Working knowledge of ICH-GCP guidelines, study protocols, and Indian regulatory requirements (CDSCO, etc.)
- Excellent attention to detail, organizational skills, and communication abilities
- Experience in clinical trial site operations preferred
Key Responsibilities
- Manage daily site activities and patient workflows
- Handle patient screening, enrollment, and follow-up coordination
- Prepare, obtain, and manage Informed Consent Forms (ICF)
- Maintain accurate and complete essential documentation
- Ensure strict compliance with study protocols and ICH-GCP standards
- Liaise with investigators, CRAs, sponsors, and internal teams
- Support data entry, query resolution, and site readiness for audits/inspections
Benefits / Perks
- Opportunity to work with a leading SMO in India’s growing clinical research sector
- Hands-on experience in multi-site trial management and regulatory compliance
- Professional development in ICH-GCP and clinical operations
- Supportive environment focused on precision, timelines, and quality
- Contribution to advancing innovative therapies through ethical research
- Stable role in Nagpur with potential for growth in clinical research
How to Apply
Send your updated resume via email to: contact@hrapl.in
Email Subject Line: [Your Name]_CRC_Nagpur
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the HRAPL LinkedIn page.
For more clinical research jobs, CRC opportunities, and pharma/biotech roles in India, visit Pharma Recruiter.
Note: This is an email-based application; no walk-in mentioned—apply promptly as there is only 1 opening.
Why You Should Join HRAPL
HRAPL stands out as a pioneer SMO in India, offering a platform to build expertise in clinical trial site management with a strong emphasis on excellence, innovation, and ethical practices.
Located in Nagpur, this role provides meaningful work in advancing global healthcare through precise, compliant trial execution. Join a committed team that values timelines, quality, and professional growth in the dynamic field of clinical research.
FAQs
What qualifications are required for the Clinical Research Coordinator role at HRAPL?
Graduate degree in Life Sciences, Biotechnology, Pharmacy, or related fields, plus 2-3 years in clinical trial site operations.
Is experience in ICH-GCP mandatory?
Working knowledge of ICH-GCP, protocols, and regulatory requirements is essential; prior site experience strengthens your application.
How do I apply for this CRC position in Nagpur?
Email your resume to contact@hrapl.in with subject line: [Your Name]_CRC_Nagpur.
What makes HRAPL a good choice for clinical research careers?
As a leading SMO with ISO certification, HRAPL offers exposure to comprehensive trial services, multi-site coordination, and a focus on quality and innovation in India.
