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Company Description QREC Clinical Research LLP is a global Contract Research Organization with offices in Jaipur and Hyderabad in India, and Dubai in the UAE, providing comprehensive clinical research and medico-marketing services to healthcare organizations, doctors, and researchers across government and private sectors. The company specializes in Phase 3 and 4 clinical trials, real-world and observational studies, post-marketing surveillance, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico-marketing projects. QREC has delivered hundreds of end-to-end studies and projects, contributing to brand plans, scientific publications, regulatory submissions, and medical device research. With a large database of doctors and patients, numerous publications, and a skilled multidisciplinary team, QREC maintains a strong track record of quality, including zero major observations in sponsor and independent audit reports. The organization offers opportunities to work on diverse therapeutic areas and international projects in a structured, data-driven environment.
Role Description This is a full-time, on-site Clinical Project Associate role based in Jaipur, Rajasthan. The Clinical Project Associate will support the planning, coordination, and execution of clinical trials and real-world studies in pharmacy, dental, and life sciences domains. Day-to-day responsibilities include assisting in protocol implementation, maintaining study documentation, coordinating with investigators and site staff, and helping ensure adherence to regulatory and ethical guidelines. The role involves tracking project timelines and deliverables, supporting data collection and query resolution, and collaborating with cross-functional teams such as data management, medical writing, and statistics. The Clinical Project Associate will also contribute to site training activities, support communication between internal and external stakeholders, and participate in quality and compliance processes as required.
Qualifications
Candidates should possess strong Analytical Skills, including data interpretation, attention to detail, and problem-solving abilities.
Candidates should possess effective Communication skills, including clear written and verbal communication and the ability to collaborate with investigators, site teams, and internal stakeholders.
Candidates should possess Project Management skills, such as organizing tasks, tracking timelines, managing documentation, and supporting study coordination.
Candidates should possess Training-related skills, including the ability to assist in site initiation, educate site staff on study procedures, and support internal knowledge-sharing.
Candidates should possess Research skills, including familiarity with clinical research processes, literature review, and basic understanding of study design and GCP principles.
Bachelor’s or Master’s degree in Pharmacy, Dental, Life Sciences, or a related healthcare field.
Prior internship or experience in clinical research, CRO, hospital research department, or related domain is preferred.
Good proficiency in MS Office tools and basic clinical data documentation practices.
Work arrangement
No
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