Looking for pharma jobs in India, clinical research jobs, QA jobs, QC jobs, or exciting pharmaceutical careers in India? HRAPL is currently hiring an experienced Clinical Research Coordinator in Nagpur, Maharashtra.
Contents
About the Company
HRAPL is a growing organization operating in the clinical research and healthcare sector. The company is committed to maintaining high standards of quality, regulatory compliance, and operational excellence in clinical trials.
With a strong focus on innovation, patient safety, and research integrity, HRAPL provides professionals with opportunities to contribute to impactful healthcare advancements while building rewarding long-term careers.
Organizations like HRAPL continue to play an important role in strengthening India’s clinical research ecosystem through ethical practices, regulatory adherence, and efficient study management.
Job Details
- Company Name: HRAPL
- Position: Clinical Research Coordinator (CRC)
- Experience: 2–3 Years
- Qualification: Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields
- Location: Nagpur, Maharashtra, India
- Work Type: On-site
- Open Positions: 1
- Joining Preference: Immediate Joiners Preferred
Job Description
HRAPL is seeking an experienced Clinical Research Coordinator to oversee day-to-day clinical trial operations and ensure smooth execution of site activities.
The selected candidate will be responsible for patient coordination, documentation management, protocol compliance, and collaboration with study stakeholders.
Clinical Research Coordinator
- Department: Clinical Research Operations
- Market: Clinical Research and Healthcare
- Role: Clinical Research Coordinator
- Experience: 2–3 Years
- Education/Qualification: Graduate in Life Sciences, Biotechnology, Pharmacy, or related disciplines
Skills and Qualifications
- Graduate degree in Life Sciences, Biotechnology, Pharmacy, or related fields
- 2–3 years of clinical trial site operations experience
- Strong patient coordination skills
- Experience handling Informed Consent Forms (ICF)
- Knowledge of essential clinical documentation
- Understanding of ICH-GCP guidelines
- Familiarity with study protocols and regulatory requirements
- Excellent communication and coordination abilities
- Strong attention to detail
- Ability to collaborate with investigators and CRAs
Key Responsibilities
- Coordinate daily clinical trial activities
- Manage patient scheduling and follow-ups
- Maintain accurate trial documentation
- Ensure protocol compliance at study sites
- Support investigator and CRA coordination
- Handle informed consent documentation
- Monitor site operational efficiency
- Ensure regulatory compliance standards
- Maintain study records and files
- Support quality clinical operations
Benefits and Perks
- Career growth in clinical research
- Exposure to industry-standard clinical practices
- Learning opportunities in regulated environments
- Professional development and skill enhancement
- Collaborative work culture
- Opportunity to work with experienced research professionals
- Long-term career prospects in healthcare research
- Exposure to regulatory and compliance frameworks
How to Apply
Interested candidates who meet the eligibility requirements should submit their updated resume directly to the official HRAPL recruitment email.
Email: contact@hrapl.in
Email Subject Line: Name_CRC_Nagpur
Candidates are encouraged to apply as early as possible, especially immediate joiners, as only one position is currently available.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Hrapl career page.
For additional pharmaceutical job openings and industry updates, visit Pharma Recruiter.
Apply today and take the next step in your clinical research career.
Why You Should Join HRAPL
HRAPL offers professionals an opportunity to work in a structured and compliance-driven clinical research environment. Employees gain valuable exposure to clinical trial operations, patient management, regulatory processes, and cross-functional collaboration.
FAQs
Who is eligible to apply for this Clinical Research Coordinator position?
Candidates with a degree in Life Sciences, Biotechnology, Pharmacy, or related fields and 2–3 years of clinical trial experience are eligible.
How can I apply for this job?
Interested applicants should send their updated resume to contact@hrapl.in using the subject line Name_CRC_Nagpur.
Is this a walk-in interview opportunity?
No walk-in interview details have been provided. Candidates should apply through the official email address.
What career growth opportunities are available?
The role offers exposure to clinical trial management, regulatory compliance, patient coordination, and broader clinical research operations, supporting long-term career development.
