QREC Clinical Research LLP – Jaipur, Rajasthan
QREC Clinical Research LLP is a rapidly growing Contract Research Organization (CRO) with operations across India and the UAE, delivering specialized services in Clinical Research, Medical Writing, Regulatory Affairs, Clinical Data Management, Biostatistics, and Healthcare Analytics.
With experience across 810+ statistical projects and 360+ regulatory submissions, QREC collaborates with hospitals, healthcare organizations, researchers, and pharmaceutical companies globally.
We are currently hiring motivated and detail-oriented professionals for the position of Clinical Process Associate at our Jaipur office.
Position Details
Job Title: Clinical Process Associate
Location: Jaipur, Rajasthan
Employment Type: Full-Time
Work Mode: On-site
Industry: Clinical Research / Healthcare / CRO
Eligibility Criteria
Candidates from the following educational backgrounds may apply:
- B.Pharm / M.Pharm
- BDS / MDS
- B.Sc / M.Sc (Life Sciences)
- Biotechnology / Microbiology / Biochemistry
- Pharma & Healthcare-related backgrounds
Experience
- Freshers with strong communication and learning abilities are encouraged to apply.
- Candidates with prior experience as a Clinical Research Coordinator (CRC) will be preferred.
Key Responsibilities
The selected candidate will be involved in clinical research operations and project coordination activities, including:
- Assisting in clinical trial and research-related operational activities
- Coordinating clinical research projects and site-related activities
- Supporting clinical documentation and clinical data management processes
- Maintaining study records, regulatory files, and essential documentation
- Assisting in patient coordination, follow-up, and study tracking activities
- Coordinating with internal departments for smooth project execution
- Assisting in medical writing, publication support, and research documentation
- Handling project tracking, reporting, and operational updates
- Supporting budgeting and project coordination activities
- Ensuring compliance with ICH-GCP guidelines and regulatory standards
- Communicating professionally with clients, investigators, and stakeholders
- Collaborating with cross-functional teams including Regulatory Affairs, Data Management, Biostatistics, and Medical Writing departments
Required Skills
- Strong communication and interpersonal skills
- Good analytical and documentation abilities
- Basic understanding of clinical research processes
- Ability to work in a team-oriented environment
- Good knowledge of MS Office and professional documentation
- Willingness to learn and grow in the CRO industry
Preferred Skills
Candidates with exposure to the following areas will have an added advantage:
- Clinical Trials
- Clinical Research Coordination (CRC)
- ICH-GCP Guidelines
- Regulatory Submissions
- Medical Writing
- Clinical Data Management
- Publication Support
- Healthcare Process Coordination
Why Join QREC?
At QREC, we focus on creating a learning-driven and growth-oriented environment for healthcare professionals.
What You Will Gain:
- Exposure to global clinical research projects
- Hands-on experience in CRO operations
- Learning opportunities in Medical Writing and Regulatory Affairs
- Professional development and mentorship
- Opportunity to work with multidisciplinary healthcare teams
- Long-term career growth in the Clinical Research industry
How to Apply
Interested candidates can share their updated resume at: [email protected]
Pay: ₹20,000.00 - ₹22,000.00 per month
Work Location: In person
