clinical study coordinator

Company Description

QREC Clinical Research LLP is a Contract Research Organisation with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE). The company offers comprehensive services to the healthcare industry, doctors, and researchers in clinical trials (Phase 3 & 4), REAL WORLD studies, observational studies, PMS, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico marketing globally. QREC has successfully completed numerous projects, including 450+ brand plans, 162+ REAL World studies, and 810+ statistical analysis projects, supported by a database of 45,000+ doctors and 8,10,000+ patients.

Role Description

This is a full-time on-site role for a Clinical Study Coordinator, located in Jaipur. The Clinical Study Coordinator will be responsible for daily tasks such as coordinating and managing clinical trials, obtaining informed consent from participants, ensuring adherence to protocols, and conducting research. The role includes responsibilities such as data collection, maintaining study documentation, overseeing regulatory compliance, and collaborating with investigators and clinical staff.

Qualifications

• Experience in Informed Consent and Protocol adherence
• Clinical Research Experience and Clinical Trials management skills
• Strong research and data collection abilities
• Excellent organizational and documentation skills
• Knowledge of regulatory compliance and guidelines
• Effective communication and collaboration skills
• Bachelor's degree in Clinical Research, Life Sciences, or a related field
• Experience in the healthcare industry is a plus