Clinical Trials Associate

Clinical Trial Associate (CTA) Location: Jaipur, Rajasthan (Work from Office) Job Type: Full-Time About QREC Clinical Research LLP QREC Clinical Research LLP is a rapidly growing Contract Research Organization (CRO) specializing in Clinical Research, Medical Writing, Regulatory Affairs, Clinical Data Management, Biostatistics, and Healthcare Analytics. We are committed to delivering high-quality research solutions for national and international healthcare organizations while fostering a collaborative, learning-driven, and growth-oriented work environment. We are looking for enthusiastic, detail-oriented, and career-driven professionals to join our Clinical Operations team as a Clinical Trial Associate (CTA). This role offers an excellent opportunity for fresh graduates and experienced professionals to gain hands-on experience in the clinical research industry while working on national and international healthcare projects. Candidates from Rajasthan will be given preference. Key Responsibilities As a Clinical Trial Associate (CTA), you will be responsible for: Supporting day-to-day clinical trial operations and project activities.Maintaining Trial Master File (TMF), Investigator Site Files (ISF), and other essential clinical trial documentation.Assisting in study start-up, site activation, study tracking, and close-out activities.Coordinating with internal teams, investigators, sponsors, ethics committees, and other stakeholders.Preparing, reviewing, and maintaining study-related reports and documentation.Supporting medical writing, publication support, and clinical documentation activities, as required.Tracking project timelines and ensuring timely completion of assigned tasks.Ensuring compliance with ICH-GCP guidelines, SOPs, and applicable regulatory requirements.Assisting in data review, quality checks, and documentation management.Communicating professionally with clients and stakeholders while maintaining confidentiality and data integrity.Eligibility B.Pharm / M.PharmBDS / MDSB.Sc / M.Sc (Life Sciences)M.Sc BiotechnologyMicrobiologyBiochemistryOther Healthcare or Pharmacy-related disciplinesRequired Skills Strong English communication skills (written and verbal).Good computer knowledge, including proficiency in MS Office (Word, Excel, PowerPoint, and Outlook).Strong analytical, organizational, and documentation abilities.Excellent interpersonal, coordination, and communication skills.Basic understanding of Clinical Research, Clinical Trial processes, and ICH-GCP guidelines (preferred).Ability to learn quickly and work in a fast-paced, deadline-driven environment.Positive attitude, attention to detail, and willingness to build a long-term career in the Clinical Research/CRO industry.Preferred Experience Candidates with prior experience as a Clinical Trial Associate (CTA), Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Clinical Trial Assistant, or Site Executive will be preferred.Exposure to Clinical Trials, Regulatory Affairs, Medical Writing, Clinical Data Management, Trial Master File (TMF) management, or Publication Support will be an added advantage.Why Join QREC Exposure to real-time national and international clinical research projects.Hands-on learning in Clinical Operations, Medical Writing, Regulatory Affairs, Clinical Data Management, and Healthcare Analytics.Structured training, professional mentorship, and career development opportunities.Opportunity to work with experienced clinical research professionals.Dynamic, collaborative, and learning-focused work environment.Long-term career growth in the Clinical Research and CRO industry.Location: Jaipur, Rajasthan (Work from Office) Employment Type: Full-Time Join QREC Clinical Research LLP and build your career in the fast-growing world of Clinical Research and Clinical Trials. Compensation: 18,000.00 - 25,000.00 per month Work Location: In person .