QREC Clinical Research LLP, a growing Contract Research Organization (CRO) with offices in India and the UAE, is hiring a Clinical Process Associate in Jaipur, Rajasthan. This opportunity is ideal for B.Pharm, M.Pharm, Life Sciences, and Dental graduates who want to start or grow their careers in clinical research operations, data management, and regulatory documentation.
QREC supports global healthcare organizations with services including Phase III & IV clinical trials, real-world evidence studies, regulatory submissions, clinical data management, medical writing, and statistical analysis. With over 810 statistical projects and 360+ regulatory submissions, the organization has built a strong reputation in global clinical research services.
This clinical research job in Jaipur offers candidates exposure to clinical trial processes, CRO operations, and regulatory compliance frameworks, making it an excellent opportunity for freshers or early-career professionals in the pharmaceutical and life sciences domain.
Job Overview
Position: Clinical Process Associate
Company: QREC Clinical Research LLP
Location: Jaipur, Rajasthan, India
Employment Type: Full-time
Work Mode: On-site
Industry: Clinical Research / CRO / Healthcare
Key Responsibilities
The Clinical Process Associate will support clinical research operations and project management activities across multiple studies.
Primary responsibilities include:
โข Assist in clinical trial operations and monitoring activities
โข Support clinical data management and documentation processes
โข Coordinate with internal teams for clinical project execution
โข Maintain study documentation and regulatory compliance records
โข Handle client communication and stakeholder queries
โข Support project reporting and operational tracking
โข Assist in clinical study budgeting and finance-related documentation
โข Ensure compliance with ICH-GCP guidelines and regulatory requirements
โข Collaborate with cross-functional teams including data management, medical writing, and regulatory affairs
Required Qualifications
Candidates applying for this clinical research associate-level role should meet the following criteria:
โข Bachelorโs or Masterโs degree in Pharmacy, Life Sciences, Dentistry, or related healthcare field
โข Strong analytical skills for evaluating clinical data
โข Excellent communication and stakeholder coordination skills
โข Basic understanding of clinical research processes and regulatory guidelines
โข Familiarity with clinical research operations or BPO workflows
โข Ability to work effectively in team-based CRO environments
Preferred Skills
Candidates with the following experience will have an advantage:
โข Knowledge of clinical trials and research documentation
โข Understanding of ICH-GCP, regulatory submissions, and observational studies
โข Exposure to clinical data management or medical writing
โข Experience in healthcare customer support or CRO project coordination
Why Join QREC Clinical Research LLP
Working at QREC offers exposure to global clinical research projects and multidisciplinary teams.
Key benefits include:
โข Opportunity to work in a global CRO environment
โข Hands-on exposure to clinical trials and regulatory submissions
โข Experience across data management, medical writing, and research operations
โข Career development in clinical research and healthcare analytics
โข Collaboration with international healthcare clients and researchers
How to Apply
You can Share ur Resume on this : HRQRECCRO@qreccr.com
