The Clinical Trial Coordinator plays a critical role in supporting the planning, implementation, and management of clinical trials. They work closely with various stakeholders, including principal investigators, study teams, regulatory bodies, and sponsors, to ensure the smooth execution of clinical research studies.
Key Responsibilities
- Study Planning and Documentation: Assist in the development of study protocols, CRF, ICR, and other study-related documentation.
- Study Coordination: Coordinate and schedule study-related activities, including participant recruitment, screening, enrollment, and follow-up visits. Liaise with study sites, investigators, and research staff to provide guidance and support for study implementation.
- Data Collection and Management: Oversee data collection activities, including the development and implementation of data collection tools and systems. Ensure accurate and timely entry of study data into the electronic data capture (EDC) system or other designated databases. Perform data quality checks and resolve data discrepancies in collaboration with the data management team.
- Study Monitoring and Reporting: Assist in monitoring the progress of clinical trials, ensuring adherence to timelines and study milestones. Contribute to the preparation of study reports, presentations, and publications.
Qualifications And Skills
- Minimum qualification is Bachelor's degree in life sciences, nursing, pharmacy, or a related discipline. Master's or Ph. D qualification is preferred for certain positions.
- Prior experience in clinical research as clinical trial coordination is highly desirable.
- Must have knowledge of Good Clinical Practice (GCP) guidelines, applicable regulatory requirements (e.g., Indian, FDA, EMA), and ethical considerations in human subjects research.
- Familiarity with electronic data capture (EDC) systems and other clinical trial management tools.
- Proficiency in using common software applications (e.g., Microsoft Office suite, data analysis tools).
- Flexibility and adaptability to navigate changing priorities and evolving study requirements.
Patanjali Research Foundation is an equal opportunity employer and does not discriminate against any applicant because of race, colour, religion, gender, national origin, age and physical disability.
How To Apply
- Write to [Confidential Information] with your detailed CV and career aspirations.
- Mention Clinical Trial Coordinator/Site Monitor , citing respective Job Code.
- List three professional references other than your friends and family.
