QREC Clinical Research LLP has announced a new Clinical Process Associate job in Jaipur for candidates interested in building a career in clinical research and CRO operations. The full-time, on-site opportunity is open to B.Pharm, M.Pharm, BDS, MDS, B.Sc, M.Sc and other life sciences candidates, with freshers also encouraged to apply.
Candidates selected for the QREC Clinical Research hiring drive will gain exposure to clinical research operations, clinical documentation, project coordination, clinical data management, medical writing and regulatory activities. Applicants with previous Clinical Research Coordinator (CRC) experience will receive preference.
QREC Clinical Research Job Overview
| Particulars | Details |
|---|---|
| Company | QREC Clinical Research LLP |
| Job Role | Clinical Process Associate |
| Location | Jaipur, Rajasthan |
| Industry | Clinical Research / Healthcare / CRO |
| Employment Type | Full-Time |
| Work Mode | On-site |
| Experience | Freshers can apply; CRC experience preferred |
| Salary | ₹18,000 – ₹22,000 per month |
| Application Mode |
About QREC Clinical Research LLP
QREC Clinical Research LLP is a Contract Research Organization (CRO) operating across India and the UAE. According to the employer-provided job description, the organization provides specialized services across Clinical Research, Medical Writing, Regulatory Affairs, Clinical Data Management, Biostatistics and Healthcare Analytics.
The company states that it has experience involving more than 810 statistical projects and 360 regulatory submissions, while working with hospitals, healthcare organizations, researchers and pharmaceutical companies.
Clinical Process Associate Job Description
The Clinical Process Associate at QREC Clinical Research will support clinical research operations and project coordination activities.
The position provides exposure to multiple functions within the CRO environment, including clinical trial operations, clinical documentation, regulatory processes, clinical data management, medical writing and project tracking.
This makes the opportunity particularly relevant for fresh graduates who want to start a career in clinical research in Jaipur.
Key Responsibilities
Selected candidates may be responsible for:
- Assisting with 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 clinical trial documentation.
- Assisting with patient coordination, follow-up and study tracking.
- Coordinating with internal departments for smooth execution of clinical research projects.
- Supporting medical writing, publication activities and research documentation.
- Managing project tracking, reports and operational updates.
- Supporting budgeting and project coordination activities.
- Following applicable ICH-GCP guidelines and regulatory requirements.
- Communicating professionally with clients, investigators and other stakeholders.
- Working with cross-functional teams in Regulatory Affairs, Clinical Data Management, Biostatistics and Medical Writing.
Who Can Apply?
Candidates with the following educational qualifications are eligible to apply for the QREC Clinical Process Associate vacancy:
- B.Pharm
- M.Pharm
- BDS
- MDS
- B.Sc in Life Sciences
- M.Sc in Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Other relevant pharmaceutical and healthcare-related educational backgrounds
Fresh graduates with good communication skills, an interest in clinical research and a willingness to learn are encouraged to apply.
Candidates who have previously worked as a Clinical Research Coordinator (CRC) will be preferred.
Skills Required
Candidates applying for the Clinical Process Associate position should ideally have:
- Strong communication and interpersonal skills
- Good analytical and documentation abilities
- Basic understanding of clinical research processes
- Ability to collaborate effectively in a team
- Working knowledge of MS Office
- Professional documentation skills
- Willingness to learn clinical research and CRO processes
Preferred Clinical Research Skills
Exposure to any of the following areas may provide candidates with an additional advantage:
Clinical Trials | Clinical Research Coordination | ICH-GCP | Regulatory Submissions | Medical Writing | Clinical Data Management | Publication Support | Healthcare Process Coordination
Candidates do not necessarily need experience across all these areas, particularly where applying as freshers.
Salary
QREC Clinical Research LLP has listed a salary of:
₹18,000 – ₹22,000 per month
This corresponds to approximately ₹2.16 lakh – ₹2.64 lakh per year, before considering any other components or deductions that may apply.
Candidates should confirm the final compensation structure directly with the employer during the recruitment process.
Why Join QREC Clinical Research?
According to the job description, selected candidates can gain:
- Exposure to global clinical research projects
- Hands-on experience with CRO operations
- Learning opportunities in Medical Writing and Regulatory Affairs
- Professional development and mentorship
- Experience working with multidisciplinary healthcare teams
- Opportunities for long-term career development within clinical research
The multidisciplinary nature of the position may be particularly useful for candidates seeking early-career exposure before specializing in areas such as Clinical Operations, CRC, Clinical Data Management, Regulatory Affairs or Medical Writing.
How to Apply for QREC Clinical Research Jobs
Interested and eligible candidates can prepare an updated resume highlighting their educational qualifications, clinical research knowledge, internships, projects and any relevant CRC or CRO experience.
Application Email: hrqreccro@qreccr.com
Candidates should mention the Clinical Process Associate position clearly while submitting their application.