Blog
Clinical Trial Associate Job at QREC Clinical Research LLP
QREC Clinical Research LLP (India–UAE), a reputed global Contract Research Organisation (CRO), is hiring a Clinical Trial Associate for its Jaipur, Rajasthan office. This is a full-time, on-site clinical research job offering hands-on exposure to Phase III & IV clinical trials, TMF management, informed consent processes, and regulatory compliance.
With operational hubs in Jaipur, Hyderabad, and Dubai, QREC supports pharmaceutical companies, government healthcare initiatives, and private sponsors through clinical trials, real-world evidence studies, and observational research. The organization is known for its strong audit record and high-quality regulatory submissions.
This opportunity is ideal for Life Sciences and Pharmacy graduates seeking to build a long-term career in clinical operations and CRO environments.
Key Responsibilities – Clinical Trial Associate
- Coordinate day-to-day clinical trial activities in compliance with protocols and SOPs
- Manage and maintain Trial Master Files (TMF) (paper/eTMF)
- Assist in Informed Consent Process (ICF) documentation and compliance
- Support investigators, sponsors, and internal clinical research teams
- Ensure adherence to GCP, ICH guidelines, and regulatory requirements
- Assist in site documentation, audit readiness, and trial tracking
- Support clinical operations across Phase III and Phase IV studies
Eligibility & Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy (B.Pharm/M.Pharm), or related discipline
- Knowledge of clinical trials, clinical operations, and research methodologies
- Experience or familiarity with TMF management and informed consent processes
- Understanding of GCP (Good Clinical Practice) guidelines
- Strong organizational, documentation, and communication skills
- Ability to collaborate with multidisciplinary clinical research teams
- Certification in clinical research (ACRP, ICH-GCP, etc.) is an added advantage
Eligible Locations
Candidates from Rajasthan, Uttar Pradesh, Haryana, Madhya Pradesh, Delhi, Uttarakhand, and Punjab may apply.
Salary & Benefits
- Estimated Salary Range: ₹3,00,000 – ₹5,50,000 per annum (INR)
- Hands-on exposure to regulated clinical trials
- Career growth in a global CRO environment
- Opportunity to work on regulatory-compliant, audited projects
- Collaborative and research-driven work culture
(Salary may vary based on qualifications and prior experience.)
How to Apply
