QREC Clinical Research LLP is recruiting for the position of Clinical Research Associate (CRA) in Jaipur, Rajasthan. Candidates with 0–2 years of experience, including freshers interested in clinical research and clinical trial operations, can apply.
The position offers an opportunity to work with clinical operations teams and gain exposure to clinical research projects, study documentation, site coordination, and regulatory compliance. Candidates from Rajasthan will be preferred.
QREC Clinical Research Associate Recruitment 2026: Job Details
| Particulars | Details |
|---|---|
| Company | QREC Clinical Research LLP |
| Job Role | Clinical Research Associate (CRA) |
| Department | Clinical Operations |
| Job Location | Jaipur, Rajasthan |
| Work Mode | On-site / Work from Office |
| Employment Type | Full-time |
| Experience | 0–2 years |
| Salary | ₹18,000–₹22,000 per month |
| Preferred Candidates | Candidates from Rajasthan |
| Suitable Candidates | Freshers and experienced applicants |
Position: Clinical Research Associate (CRA)
The Clinical Research Associate will support clinical trial activities, coordinate with study sites and investigators, maintain essential study documentation, track project timelines, and help ensure compliance with study protocols, standard operating procedures (SOPs), and applicable regulatory requirements.
Key Responsibilities
- Support clinical trial activities in accordance with study protocols, SOPs, and regulatory requirements.
- Coordinate with clinical study sites, investigators, internal teams, and other stakeholders.
- Assist with site communication, follow-ups, documentation, and trial-related activities.
- Review and maintain essential clinical trial documents and study records.
- Track study progress, timelines, pending activities, and site deliverables.
- Prepare and review study reports, trackers, presentations, and clinical research documents.
- Follow up on study-related queries, deviations, and action items.
- Maintain data integrity, confidentiality, and compliance.
- Coordinate with Medical Writing, Regulatory Affairs, Clinical Data Management, and Biostatistics teams.
- Develop knowledge of ICH-GCP and clinical research practices through training.
Eligibility Criteria and Educational Qualifications
Candidates with the following educational backgrounds can apply:
- B.Pharm / M.Pharm
- BDS / MDS
- B.Sc / M.Sc in Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Other relevant Pharmacy, Healthcare, or Life Sciences disciplines
Experience: 0–2 years. Freshers with a strong interest in clinical research are encouraged to apply.
Candidates with previous exposure to clinical research, clinical trial projects, or related functions will be preferred.
Preferred Experience
Experience or exposure in any of the following areas is beneficial:
- Clinical Research Associate (CRA)
- Clinical Research Coordinator (CRC)
- Clinical Trial Assistant (CTA)
- Site Executive or Clinical Operations
- Clinical Trials and Clinical Research Projects
- Regulatory Affairs
- Medical Writing
- Clinical Data Management
- Publication Support
Required Skills
- Strong written and verbal English communication.
- Working knowledge of MS Office, including Word, Excel, PowerPoint, and Outlook.
- Documentation and organizational skills.
- Site coordination, follow-up, and professional communication.
- Familiarity with or willingness to learn ICH-GCP, clinical trial processes, and regulatory requirements.
- Analytical thinking and the ability to manage multiple tasks.
- A proactive approach and willingness to learn.
Salary and Career Opportunities
The selected candidates will receive a salary of ₹18,000–₹22,000 per month.
The role provides exposure to national and international healthcare projects, clinical trial operations, multidisciplinary teams, and related functions such as Medical Writing, Regulatory Affairs, Clinical Data Management, and Biostatistics.
How to Apply
