Clinical Trial Specialist

QREC Clinical Research LLP, a Contract Research Organization, operates from Jaipur (India), Hyderabad (India), and Dubai (UAE) to deliver comprehensive services to the healthcare industry, doctors, and researchers in clinical trials (Phase 3 and 4), real-world and observational studies, post-marketing surveillance (PMS), medical writing, clinical data management, and statistical analysis. With a proven track record, QREC has completed over 450 brand plans, 162 real-world studies, 153 investigator-initiated studies, and numerous regulatory submissions, publication projects, and medical device studies globally. Supported by a robust database of over 45,000 doctors and 810,000 patients, QREC is backed by a skilled team of 63 professionals and has maintained excellence with zero major observations during sponsor and independent audits.

This is a full-time on-site role for a Clinical Trial Specialist located in Jaipur. The Clinical Trial Specialist will oversee day-to-day management of clinical trials, ensuring protocol adherence, managing clinical operations, and coordinating with Institutional Review Boards (IRBs). Responsibilities include supporting study design, monitoring study process compliance, collecting and analyzing clinical data, and collaborating with research teams to ensure successful trial execution while adhering to regulatory requirements and ethical standards.

• Knowledge of Protocol design and implementation for clinical trials
• Experience in Clinical Operations, including trial management and regulatory compliance
• Familiarity with Clinical Trials and Research methodologies
• Understanding of Institutional Review Boards (IRB) and their guidelines
• Attention to detail, strong organizational and communication skills
• Bachelor's degree in Life Sciences, Medical Sciences, or a related field (Master's degree preferred)
• Previous experience in the healthcare or clinical research industry is an advantage