HRAPL is hiring a Project Coordinator with 2-3 years of On-site CRA experience in Nagpur, Maharashtra. Excellent opportunity for professionals seeking pharma jobs and clinical research careers in India. Apply now!
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About the Company
Hector Research and Archival Pvt. Ltd. (HRAPL) is a leading Site Management Organization (SMO) specializing in clinical trials across India. As an ISO 9001:2015 certified company, HRAPL delivers comprehensive clinical trial management services including patient recruitment, site operations, data management, and regulatory compliance.
With a strong focus on quality, innovation, and operational excellence, HRAPL supports sponsors and CROs in conducting high-standard clinical research. The company is rapidly growing and is recognized for its precision-driven approach and commitment to advancing healthcare through efficient clinical trial execution in India.
Job Details
- Company Name: Hector Research and Archival Pvt. Ltd. (HRAPL)
- Experience: 2-3 years
- Qualification: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field
- Location: Nagpur, Maharashtra
- Work Type: On-site
Job Description
HRAPL is looking for a dynamic Project Coordinator to support clinical research operations. This role is critical in ensuring smooth project execution through effective coordination, site communication, and documentation management in ongoing clinical trials.
Project Coordinator
- Department: Clinical Operations
- Market: Clinical Research / Clinical Trials
- Role: Project Coordinator
- Experience: 2-3 years (On-site CRA)
- Education/Qualification: Bachelor’s or Master’s in Life Sciences, Pharmacy, or related field
Skills/Qualifications
- 2-3 years of On-site Clinical Research Associate (CRA) experience
- Strong organizational and multitasking abilities
- Excellent verbal and written communication skills
- Proficiency in documentation management and activity tracking
- Good understanding of clinical research processes and GCP
- Passion for high-quality clinical trial execution in India
Key Responsibilities
- Coordinate clinical research project activities
- Manage site communication and monitoring
- Handle documentation and regulatory filing
- Track project timelines and deliverables
- Support team coordination and reporting
- Ensure smooth operational execution
- Monitor site performance and compliance
Benefits/Perks
- Career growth in clinical research sector
- Learning opportunities in clinical trial management
- Competitive salary and benefits
- Professional work culture with focus on excellence
- Exposure to diverse clinical studies
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the HRAPL career page.
Interested candidates should send their updated resume to contact@hrapl.in. Important: Mention “Name_PC” in the email subject line.
For more clinical research and pharma jobs across India, visit Pharma Recruiter.
Walk-in Interview Details
No walk-in interview is scheduled. Applications are accepted only via email.
Why You Should Join
HRAPL offers a vibrant and supportive work culture that values precision, innovation, and professional growth. As a specialized SMO, the company provides long-term career stability, continuous learning in clinical research, and opportunities to contribute to meaningful healthcare advancements in a compliant and quality-focused environment.
FAQs
Q1: What experience is required for the Project Coordinator role at HRAPL?
A: 2-3 years of On-site CRA experience in clinical research.
Q2: What is the job location?
A: Nagpur, Maharashtra (On-site position).
Q3: What qualification is needed?
A: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.
Q4: How do I apply for this clinical research job?
A: Email your resume to contact@hrapl.in with subject line “Name_PC”.
Q5: How many positions are open?
A: One opening for Project Coordinator.
