QREC Clinical Research LLP is hiring for the position of Clinical Research Associate (CRA) in Jaipur, Rajasthan. This is a full-time, on-site opportunity for candidates interested in building a career in clinical research, clinical trials, and CRO operations.
The position is open to candidates with 0–2 years of experience, and freshers with a strong interest in clinical research are encouraged to apply. Candidates from Rajasthan will be preferred for this opportunity.
The advertised salary for the position is ₹18,000 to ₹22,000 per month. The role provides exposure to clinical trial activities, study documentation, site coordination, regulatory requirements, and collaboration with teams working in Medical Writing, Regulatory Affairs, Clinical Data Management, and Biostatistics.
QREC Clinical Research Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | QREC Clinical Research LLP |
| Job Title | Clinical Research Associate (CRA) |
| Job Type | Full Time |
| Location | Jaipur, Rajasthan |
| Work Mode | Work From Office / On-site |
| Experience | 0–2 Years |
| Freshers | Eligible |
| Preferred Location | Rajasthan |
| Salary | ₹18,000 – ₹22,000 per month |
| Industry | Clinical Research / CRO |
| Function | Clinical Operations |
| Application Mode | Online Application |
About QREC Clinical Research LLP
QREC Clinical Research LLP is a Contract Research Organization (CRO) working across areas such as Clinical Research, Medical Writing, Regulatory Affairs, Clinical Data Management, Biostatistics, and Healthcare Analytics.
The company has operations across India and the UAE and works on national and international healthcare-related projects.
The current opening is within the Clinical Operations team and is intended for candidates who want to develop their skills and experience in clinical research and clinical trial operations.
Job Description
The Clinical Research Associate (CRA) will support various clinical research and study-related activities.
The role involves coordination with study sites, investigators, internal teams, and other stakeholders while ensuring that assigned study activities are conducted according to protocols, SOPs, and applicable regulatory requirements.
This position can be suitable for both freshers and early-career professionals who want to establish a career in the CRO and clinical research industry.
Clinical Research Associate – Key Responsibilities
Clinical Trial Support
The CRA will assist with clinical trial activities and help ensure that study processes are performed according to:
- Study protocols
- Standard Operating Procedures (SOPs)
- Applicable regulatory requirements
- Clinical research best practices
Site and Investigator Coordination
The position includes regular coordination with:
- Clinical trial sites
- Investigators
- Internal study teams
- Other project stakeholders
The candidate will assist with site communication, follow-ups, and study-related coordination.
Clinical Trial Documentation
The CRA will help maintain and review essential clinical research documentation and study records.
Responsibilities may include:
- Maintaining study files.
- Reviewing relevant documentation.
- Following up on pending documents.
- Supporting proper record management.
- Ensuring documentation accuracy and completeness.
Study Progress Tracking
The candidate will support monitoring of study progress by tracking:
- Study timelines.
- Pending activities.
- Site deliverables.
- Follow-up items.
- Project-related tasks.
Reports and Study Documents
The role includes supporting the preparation and review of:
- Study reports.
- Trackers.
- Presentations.
- Clinical research documents.
- Other project-related materials.
Queries, Deviations and Action Items
The CRA will assist in identifying and following up on study-related:
- Queries.
- Deviations.
- Pending action items.
- Site-related issues.
Significant issues should be communicated or escalated to the appropriate team members.
Data Integrity and Confidentiality
The candidate will be expected to maintain accurate records while following requirements related to:
- Data integrity.
- Confidentiality.
- Documentation quality.
- Clinical research compliance.
Cross-Functional Collaboration
The CRA will work with multidisciplinary teams, including:
- Medical Writing
- Regulatory Affairs
- Clinical Data Management
- Biostatistics
- Clinical Operations
This provides exposure to different areas of the clinical research ecosystem.
Educational Qualification
Candidates from the following academic backgrounds can apply:
- B.Pharm
- M.Pharm
- BDS
- MDS
- B.Sc. Life Sciences
- M.Sc. Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Other relevant Healthcare, Life Sciences, or Pharmacy disciplines
The vacancy particularly encourages freshers with a strong interest in clinical research to apply.
Experience Requirements
The stated experience range is:
0–2 Years
Freshers are eligible to apply.
Candidates with previous exposure to clinical research or related functions may have relevant experience for the position.
Preferred Experience
Exposure to any of the following areas may be advantageous:
- Clinical Research Associate (CRA)
- Clinical Research Coordinator (CRC)
- Clinical Trial Assistant (CTA)
- Site Executive
- Clinical Operations
- Clinical Trials
- Clinical Research Projects
- Regulatory Affairs
- Medical Writing
- Clinical Data Management
- Publication Support
Prior experience is not mandatory for freshers according to the supplied vacancy.
Required Skills
Candidates should have:
Communication Skills
- Strong written English.
- Good verbal English.
- Professional communication skills.
- Ability to communicate effectively with different stakeholders.
Computer Skills
Candidates should be comfortable using:
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
Clinical Research Knowledge
Candidates should either have knowledge of or be willing to learn:
- ICH-GCP
- Clinical trial processes
- Clinical research practices
- Regulatory requirements
- Study documentation
Organizational Skills
The role requires:
- Attention to detail.
- Strong documentation skills.
- Good organization.
- Follow-up ability.
- Time management.
- Ability to manage multiple tasks.
Professional Attributes
QREC is looking for candidates who are:
- Analytical.
- Responsible.
- Proactive.
- Quick learners.
- Interested in clinical research.
- Comfortable working with multidisciplinary teams.
Work Location and Employment Details
Location: Jaipur, Rajasthan
Work Mode: Work From Office / On-site
Employment Type: Full Time
Preferred Candidates: Candidates based in Rajasthan are preferred.
The supplied vacancy specifically states that the work will be performed in person.
Salary / Pay
The advertised salary is:
₹18,000 – ₹22,000 per month
This corresponds to an approximate annual range of ₹2.16 lakh to ₹2.64 lakh, before considering any applicable deductions or other employment terms.
Career Development Opportunities
According to the supplied recruitment information, the role provides exposure to several areas of the clinical research ecosystem.
Potential areas of professional exposure include:
- Clinical Operations
- Clinical Trial Management
- Medical Writing
- Regulatory Affairs
- Clinical Data Management
- Biostatistics
- Healthcare Analytics
The position is intended to provide practical exposure and professional development for candidates interested in building a longer-term career in the CRO and clinical research industry.
Selection Process
The supplied vacancy does not specify a detailed selection process.
Candidates who meet the requirements may be contacted for further screening or interview stages by the recruitment team.
How to Apply
Interested candidates should apply through the recruitment listing and submit their updated resume/application as instructed.
Candidates should ensure that their educational qualifications, clinical research exposure, technical skills, and contact details are accurately mentioned in their resume.
Important Details Before Applying
- Company: QREC Clinical Research LLP.
- Position: Clinical Research Associate (CRA).
- Location: Jaipur, Rajasthan.
- Work mode: Work From Office / On-site.
- Employment: Full Time.
- Experience: 0–2 years.
- Freshers are encouraged to apply.
- Candidates from Rajasthan are preferred.
- Eligible backgrounds include Pharmacy, Life Sciences, Dentistry, Biotechnology, Microbiology, Biochemistry, and related healthcare disciplines.
- Salary: ₹18,000–₹22,000 per month.
- The role involves clinical trial support, documentation, site coordination, study tracking, and cross-functional collaboration.
- Knowledge of ICH-GCP is useful, while candidates can also develop this knowledge on the job according to the vacancy description.
Frequently Asked Questions
1. What is the job title at QREC Clinical Research?
The position is Clinical Research Associate (CRA).
2. Where is the CRA job located?
The position is based in Jaipur, Rajasthan.
3. Is this a work-from-home job?
No. The position is work from office / on-site.
4. Are freshers eligible?
Yes. The vacancy accepts candidates with 0–2 years of experience, and freshers with a strong interest in clinical research are encouraged to apply.
5. What qualifications are accepted?
Candidates from B.Pharm, M.Pharm, BDS, MDS, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, and other relevant healthcare or life sciences disciplines can apply.
6. What salary is offered?
The advertised salary is ₹18,000 to ₹22,000 per month.
7. Are Rajasthan candidates preferred?
Yes. The vacancy specifically states that candidates from Rajasthan will be preferred.
8. What will the CRA do?
The CRA will support clinical trial activities, site coordination, documentation, study tracking, reports, follow-ups, issue escalation, and compliance with protocols and applicable requirements.
9. Is knowledge of ICH-GCP required?
Candidates should be familiar with or willing to learn ICH-GCP and clinical research practices.
10. Which software skills are required?
The vacancy mentions Microsoft Word, Excel, PowerPoint, and Outlook.
11. Can candidates with Regulatory Affairs or Medical Writing exposure apply?
Yes. Previous exposure to Regulatory Affairs, Medical Writing, Clinical Data Management, Biostatistics, Clinical Operations, or related areas is listed as preferred experience.
12. Is the position full-time?
Yes. It is a full-time position.
Important Note
Recruitment requirements, vacancy status, salary, eligibility conditions, and selection procedures may change. Candidates should verify the latest information with QREC Clinical Research LLP before applying. The advertised salary and other employment terms are subject to the employer’s final offer. Meeting the eligibility criteria does not guarantee selection.