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.Pharm
- BDS / MDS
- B.Sc / M.Sc (Life Sciences)
- M.Sc Biotechnology
- Microbiology
- Biochemistry
- Other Healthcare or Pharmacy-related disciplines
Required 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.
Pay: ₹18,000.00 - ₹25,000.00 per month
Work Location: In person
