Clinical Study Associate

Company Description

QREC Clinical Research LLP, a Contract Research Organization with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE), provides comprehensive clinical research services to the healthcare industry, government, and private sectors. The company specializes in Clinical Trials (Phase 3 & 4), Real-World Evidence Studies, Post-Marketing Surveillance (PMS), Investigator-Initiated Studies, Medical Writing, Clinical Data Management, Statistical Analysis, and Medico-Marketing. With a robust global footprint, QREC has successfully delivered over 450 brand plans, 162 real-world studies, and numerous clinical data management and medical writing projects. Supported by a team of 63+ skilled professionals and a comprehensive database of over 45,000 doctors and 810,000 patients, QREC is committed to delivering high-quality, insightful outcomes for its clients worldwide.

Role Description

This is a full-time, on-site role for a Clinical Study Associate based in Jaipur. The Clinical Study Associate will be responsible for coordinating and supporting clinical trials and research projects, managing study documentation, and assisting in data collection and analysis. Responsibilities include liaising with investigators and healthcare professionals, ensuring compliance with regulatory requirements, monitoring study progress, and preparing reports. The role also entails working closely with cross-functional teams to ensure timely execution of clinical research projects.

Qualifications

• Strong communication skills to effectively interact with team members, investigators, and healthcare professionals.
• Knowledge and experience in research methodologies, study protocols, and regulatory guidelines for clinical trials.
• Background in medicine, healthcare, or a related field is preferred.
• Hands-on experience in clinical trials and familiarity with clinical trial operations is highly desirable.
• Ability to work collaboratively in a dynamic environment and adapt to new challenges.
• Detail-oriented with excellent organizational and time-management skills.
• Proficiency in medical writing and data analysis is a plus.
• Bachelor’s degree or higher in Life Sciences, Medicine, Pharmacy, or related disciplines.