Clinical Research Coordinator
2 months ago
Study Coordination: Coordinate all aspects of clinical research studies, including participant recruitment, scheduling, and follow-up visits.
- Regulatory Compliance: Ensure compliance with all relevant regulations, guidelines, and protocols governing clinical research, including hospital Ethics committee approvals.
- Informed Consent Process: Obtain informed consent from study participants, ensuring they fully understand the study's purpose, procedures, and potential risks.
- Data Collection: Collect, record, and maintain accurate and detailed data from study participants, adhering to study protocols and case report forms.
- Participant Monitoring: Monitor the health and safety of study participants throughout the research period, reporting any adverse events to the principal investigator as required.
- Clinical Procedures: Assist with clinical procedures, such as obtaining blood samples, performing medical tests, and administering study interventions, as specified in the research protocol.
- Study Documentation: Maintain organized and up-to-date study documentation, including regulatory documents, source documents, and study logs.
- Drug and Device Accountability: Ensure proper handling, storage, and dispensation of investigational drugs or medical devices, if applicable.
- Communication: Act as a liaison between the research team, study sponsors, hospital staff, and study participants to facilitate effective communication.
- Protocol Adherence: Ensure strict adherence to the study protocol and promptly report any deviations to the principal investigator.
- Data Quality Control: Conduct data quality checks to ensure accuracy and completeness of study data, resolving any discrepancies promptly.
- Study Budget Management: Assist in tracking and managing the study budget, ensuring that expenses are within the allocated budget.
- Adverse Event Reporting: Timely and accurately report any adverse events or unanticipated problems to the appropriate parties, as required by regulations and guidelines.
- Training and Education: Provide education and training to study personnel and hospital staff on study protocols, procedures, and ethical conduct.
- Protocol Amendments: Assist with protocol amendments and study updates, ensuring all study personnel are informed and implementing changes appropriately.
Study Closeout: Facilitate the closeout process of clinical research studies, ensuring all required documentation is completed and stored appropriately.
Pay: From ₹25,000.00 per month
**Education**:
- Bachelor's (required)
**Experience**:
- Research: 1 year (required)
- Clinical research: 1 year (required)
- Data collection: 1 year (required)
Work Location: In person
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