Society for Applied Studies is a Delhi-based not-for-profit research organization dedicated to conducting impactful health research and development projects. We are currently seeking candidates for the position of Coordinator for a hospital/community-based research project in Delhi.Vacancy Details
- Position: Clinical Research Coordinator
- Department: Clinical Research
- Education: B.Pharma / BDS/ BAMC/ BHMS/ MPharm
- Job Lcation : Delhi
- Experience : freshers
- Salary : Rs. 22000 Per Month
Desirable Skill & Description
skill :-
- Certificate/Diploma course in Clinical Research
- Excellent communication skills in English and Hindi
- Experience working in research settings
Description
- Coordinating with the hospital team for participant enrollment and follow-up care.
- Tracking potential participants/families for visits to the study clinic.
- Explaining study procedures to potential participants/families.
- Completing study documents, maintaining study binders, and tracking document status.
- Training participants/families in study procedures.
- Maintaining Excel trackers of participants for follow-up and study-related activities.
- Completing all study-related documents as per delegation.
Study Management:
- Coordinated and managed clinical trials from initiation through completion, ensuring adherence to study protocols, timelines, and regulatory requirements.
- Oversaw daily operations of clinical studies, including patient recruitment, enrollment, and scheduling, to ensure efficient and effective trial execution.
Patient Interaction and Support:
- Conducted informed consent processes, ensuring that participants understood the study procedures, risks, and benefits.
- Monitored and supported participants throughout the study, addressing their concerns and ensuring their compliance with study protocols.
Regulatory Compliance:
- Ensured compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines and standards.
- Prepared and submitted regulatory documents, including Institutional Review Board (IRB) applications, amendments, and safety reports.
Data Management:
- Managed and maintained accurate and complete clinical trial data, including source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
- Conducted data verification and validation to ensure data accuracy and integrity.
Site Management:
- Liaised with clinical sites to ensure adherence to study protocols, conduct site visits, and address any issues or concerns.
- Coordinated with site staff, including physicians, nurses, and laboratory personnel, to facilitate smooth study operations.
Documentation and Reporting:
- Prepared and maintained comprehensive study documentation, including study logs, patient records, and monitoring reports.
- Generated and reviewed study progress reports, highlighting key findings and addressing any deviations or issues.
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How to apply
click here to apply now :- (1) Coordinator | Society for Applied Studies, Centre for Health Research and Development | LinkedIn
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