QREC Clinical Research hiring Clinical Project Associates
- Clinical Project Associate Vacancy for Life Sciences – Jaipur
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualifications
- Skills & Competencies
- Location & Salary
- Application Process
- SEO-Focused Career Insight
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- Is prior CRO experience mandatory?
- What guidelines will I work with?
- Is this an on-site position?
- What career growth can I expect?
- Summary Table
Clinical Project Associate Vacancy for Life Sciences – Jaipur
QREC Clinical Research hiring Clinical Project Associates in Jaipur. Life Sciences & Pharmacy graduates eligible. Full-time CRO role.
QREC Clinical Research LLP is expanding its clinical operations team and inviting applications from motivated life sciences and pharmacy professionals who want to build a long-term career in clinical research project management. This opportunity is ideal for candidates who want hands-on exposure to real-world clinical studies, regulatory-compliant trial execution, and stakeholder coordination within a fast-growing Contract Research Organization. The role offers direct involvement in clinical trial operations that impact patient safety, data integrity, and regulatory success.
Company Overview
QREC Clinical Research LLP is a well-established Contract Research Organization (CRO) operating across India and the UAE, with offices in Jaipur, Hyderabad, and Dubai. The organization delivers end-to-end clinical research services to pharmaceutical, biotechnology, and healthcare companies globally. Its service portfolio includes Phase III and Phase IV clinical trials, real-world evidence studies, observational studies, post-marketing surveillance (PMS), KAP surveys, medical writing, clinical data management, and regulatory submissions.
With a professional team of over 63 experienced clinical research specialists, QREC has successfully completed multiple global and investigator-initiated studies. The company maintains access to a robust clinical ecosystem supported by a verified database of more than 45,000 doctors and over 810,000 patient records. A strong compliance culture is reflected in its consistent record of zero major observations in sponsor and independent audit reports. This credibility positions QREC as a trusted CRO partner in regulated clinical research environments.
By combining scientific rigor, regulatory compliance, and operational efficiency, QREC contributes directly to evidence-based healthcare decision-making and improved patient outcomes.
Job Role & Responsibilities
The Clinical Project Associate will play a key operational role in supporting clinical research projects from initiation through close-out. This is a full-time, on-site position based in Jaipur, suited for candidates who are detail-oriented, process-driven, and capable of managing multiple project elements simultaneously.
Key Responsibilities
- Support planning and execution of clinical research projects in accordance with approved protocols and regulatory guidelines
- Assist in maintaining project timelines, milestones, and deliverables across multiple studies
- Coordinate with internal teams, investigators, sponsors, and external stakeholders
- Support training activities related to study procedures, documentation, and compliance requirements
- Track project progress and flag risks related to timelines, quality, or compliance
- Compile, review, and maintain essential clinical trial documentation
- Ensure adherence to ICH-GCP guidelines, SOPs, and applicable regulatory requirements
- Assist in data review, reporting, and preparation of project summaries
This role strengthens practical exposure to clinical project management, CRO operations, regulatory compliance, and clinical documentation standards.
Eligibility / Qualifications
This position is suitable for candidates aiming to grow into roles such as Clinical Project Executive, Clinical Project Manager, or Clinical Operations Lead within the CRO or pharmaceutical industry.
Educational Qualifications
The following educational backgrounds are preferred:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc Life Sciences, MSc Life Sciences, BSc Biotechnology, MSc Biotechnology, BSc Clinical Research, MSc Clinical Research
Skills & Competencies
- Strong organizational and project management skills
- Ability to handle multiple clinical projects and competing deadlines
- Excellent written and verbal communication skills
- Training and coordination capabilities across cross-functional teams
- Research and analytical skills for clinical data interpretation
- Familiarity with clinical research workflows and regulatory expectations
Prior experience in clinical research, CRO operations, or healthcare research is an advantage but not mandatory for strong entry-level candidates.
Location & Salary
- Job Location: Jaipur, Rajasthan, India
- Work Mode: On-site
- Employment Type: Full-time

Application Process
Interested candidates can apply directly through the official LinkedIn job listing using the Easy Apply option.
Application Link: https://www.linkedin.com/jobs/view/4321051949
Early applications are encouraged due to limited openings and quick screening timelines.
SEO-Focused Career Insight
Clinical Project Associates act as the backbone of CRO operations, ensuring studies are delivered on time, within budget, and in compliance with global regulatory standards. With increasing clinical trial activity in India and the Middle East, experienced clinical research professionals are in strong demand across pharmaceutical sponsors, CROs, and healthcare research organizations.
This role supports long-term careers in clinical operations, regulatory affairs, clinical data management, and global clinical project leadership.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes. Candidates with relevant life sciences or pharmacy education and strong interest in clinical research can apply.
Is prior CRO experience mandatory?
No. Prior experience is advantageous but not mandatory for candidates with strong foundational knowledge.
What guidelines will I work with?
You will work under ICH-GCP guidelines, SOPs, and applicable regulatory frameworks.
Is this an on-site position?
Yes. This is a full-time, on-site role based in Jaipur.
What career growth can I expect?
This role offers progression into Clinical Project Executive, Project Manager, and senior clinical operations roles.
Summary Table
| Company | QREC Clinical Research LLP |
|---|---|
| Vacancies | Clinical Project Associate |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc Life Sciences, MSc Life Sciences, BSc Biotechnology, MSc Biotechnology, BSc Clinical Research, MSc Clinical Research |
| Experience | Freshers to Experienced |
To apply for this job please visit www.linkedin.com.