Clinical Trial Site Management Associate

Company Description

QREC Clinical Research LLP is a Contract Research Organization (CRO) offering comprehensive services to the healthcare industry, doctors, and researchers within both government and private sectors. With offices in Jaipur (India), Hyderabad (India), and Dubai (UAE), QREC specializes in Clinical Trials (Phase 3 & 4), Real-World and Observational Studies, Post-Marketing Surveillance (PMS), Investigator Initiated Studies, Medical Writing, Clinical Data Management, Statistical Analysis, and Medico-Marketing on a global scale. Its extensive expertise is demonstrated through 450+ brand strategies, 9+ global studies, 810+ statistical analysis projects, and access to a database of over 45,000 doctors and 810,000 patients across various therapeutic areas. QREC is committed to quality, delivering impactful scientific data and maintaining a perfect audit record.

Role Description

This is a full-time, on-site role for a Clinical Trial Site Management Associate, based in Jaipur, India. The responsibilities include overseeing clinical trial site operations, ensuring trials comply with regulatory and protocol requirements, and serving as a communication conduit between site staff and research sponsors. Additional duties involve managing participant recruitment, monitoring patient safety and data quality, maintaining documentation, and providing training to site personnel to ensure adherence to research protocols.

Qualifications

• Proficiency in Clinical Trial Management, including site operations and patient recruitment
• Familiarity with regulatory and compliance standards in clinical research, such as ICH-GCP guidelines
• Experience in documentation, report preparation, and maintaining trial records accurately
• Strong communication and interpersonal skills to liaise effectively with site staff and sponsors
• Analytical and problem-solving skills for data monitoring and quality control
• Ability to manage multiple tasks efficiently and work collaboratively in team settings
• Preferred: Bachelor’s degree in Life Sciences, Pharmacy, or a related field, and prior experience in clinical research