Clinical Trial Site Management Associate

Company Description

QREC Clinical Research LLP is a Contract Research Organisation (CRO) providing comprehensive clinical research services globally, with offices in Jaipur and Hyderabad, India, as well as Dubai, UAE. The company specializes in clinical trials (Phase 3 & 4), observational studies, real-world evidence studies, investigator-initiated research, clinical data management, medical writing, and more. QREC has a proven track record of delivering excellence in healthcare industry support, including global studies, regulatory submissions, and publications, with zero major observations in sponsor and independent audit reports. Backed by a team of skilled professionals, an extensive doctor and patient database, and significant study contributions, QREC is committed to advancing medical research and innovation.

Role Description

This is a full-time on-site role for a Clinical Trial Site Management Associate located in Jaipur, India. The role entails managing activities related to clinical trial sites, monitoring site compliance, maintaining regulatory documentation, and coordinating with site administrators and principal investigators. Candidates will oversee patient recruitment, ensure adherence to trial protocols, and assist in resolving any site-specific challenges, contributing to the successful execution of clinical studies. Collaboration with internal teams to address project needs is also an integral part of this role.

Qualifications

• Experience in clinical trial site operations, monitoring site adherence to protocols, regulatory compliance, and report generation.
• Keen understanding of clinical research processes, regulatory guidelines, and patient recruitment strategies.
• Strong organizational, communication, and problem-solving skills with the ability to manage multiple priorities effectively.
• Proficiency in maintaining documentation and coordinating with healthcare professionals within clinical research environments.
• Familiarity with Good Clinical Practice (GCP) guidelines and global clinical trial standards.
• Bachelor's degree in Healthcare, Life Sciences, Pharmacy, or a related field is preferred.
• Prior experience in an on-site clinical trials setting is an added advantage.