This role is well suited for professionals with prior experience as a Senior Clinical Research Associate (CRA) and exposure to study management or project coordination.
Job Overview
| Particulars | Details |
|---|---|
| Position | Project Manager |
| Company | HRAPL |
| Location | Nagpur, Maharashtra |
| Job Type | Full-Time |
| Experience | 3 - 5 years |
| Category / Department | Pharma |
| Application Mode |
🏢 About HRAPL
HRAPL is a growing Clinical Research Organization (CRO) dedicated to delivering high-quality clinical trial management and project execution services. The organization works closely with sponsors and research teams to ensure studies are conducted in accordance with global regulatory standards while maintaining quality, efficiency, and patient safety.
With a strong focus on innovation, compliance, and professional development, HRAPL offers an excellent platform for experienced clinical research professionals seeking long-term career growth.
💡 Editor's Note / Preparation Tip
This recruitment update is intended to help clinical research professionals discover verified career opportunities in project management. Applicants are advised to review the official eligibility criteria and application instructions before submitting their resumes.
📝 Job Description
HRAPL Hiring Project Manager | Clinical Research Jobs in Nagpur 2026
Company Name: HRAPL
Job Role: Project Manager
Department: Clinical Research Operations
Job Type: Full-Time
Location: Nagpur, Maharashtra
Work Mode: On-site
Experience: 3–5 Years
Qualification: Bachelor’s or Master’s Degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline
Eligibility Criteria
Applicants should possess:
* Bachelor’s or Master’s Degree in Life Sciences, Pharmacy, Biotechnology, or a related field.
* 3–5 years of experience in clinical research.
* Experience as a Senior CRA with exposure to study management or project coordination.
* Strong understanding of clinical trial operations and regulatory requirements.
Benefits & Perks
* Excellent career advancement opportunities
* Exposure to diverse clinical research projects
* Collaborative and professional work environment
* Competitive compensation package
* Leadership development opportunities
* Continuous learning and skill enhancement
* Experience working with regulatory-compliant clinical studies
* Long-term career growth in the clinical research industry
How to Apply
Interested candidates should send their updated resume to:
Email: contact@hrapl.in
Email Subject: Name_PM_Nagpur
Before applying, ensure your resume highlights your experience in clinical research, project coordination, study management, and regulatory compliance.
Apply at the earliest, as only one position is currently available.
Why You Should Join HRAPL
HRAPL provides an excellent opportunity for experienced Clinical Research Associates to transition into project management roles. Employees work on meaningful clinical research projects while gaining exposure to study leadership, regulatory compliance, and stakeholder management in a supportive and growth-oriented environment.
Advance your clinical research career with HRAPL and take the next step into project management while contributing to high-quality clinical studies in a collaborative and professional environment.
🎯 Key Responsibilities
- ✓ Lead and manage clinical research projects from planning to completion.
- ✓ Develop project plans and monitor study progress.
- ✓ Coordinate with cross-functional teams and stakeholders.
- ✓ Manage clinical study timelines and project deliverables.
- ✓ Oversee site operations and study execution.
- ✓ Ensure compliance with ICH-GCP guidelines and regulatory requirements.
- ✓ Maintain project documentation and study records.
- ✓ Track project milestones and prepare progress reports.
- ✓ Identify and resolve operational challenges.
- ✓ Ensure studies are completed within quality and timeline expectations.
💡 Required Qualifications & Skills
Frequently Asked Questions
Q1: Who can apply for this Project Manager position?
Candidates with 3–5 years of clinical research experience, particularly those who have worked as Senior Clinical Research Associates (CRA) with study management or project coordination exposure, are eligible to apply.
Q2: What qualifications are required?
Applicants should hold a Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline.
Q3: Is this a walk-in recruitment?
No. Applications are accepted only through email submission.
Q4: Where is the job located?
The position is based in Nagpur, Maharashtra.
Q5: What type of experience is preferred?
Experience in clinical trial operations, study management, site coordination, project planning, and regulatory compliance is preferred.
Q6: How should I apply?
Send your updated resume to contact@hrapl.in with the subject line Name_PM_Nagpur.
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