
Clinical Research Coordinator
6 hours ago
Eligibility:
- Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute
- Prior knowledge of the conduct of Clinical Trials,
- Phases of Clinical trials and
- Thorough Knowledge of ICH-GCP and other regulatory guidelines.
Roles and Responsibilities:
- Prepare the Database of the Investigators at the place assigned to you.
- Interact with the Investigators and know about their interest in working with us.
- Get the feasibilities completed by the Investigators in the given time.
- Collect all the necessary documents.
- Coordinates, organizes, and sets up meeting agendas, and communicates pertinent information, as required.
- Documents compile data, and distributes the notated minutes from Departmental and Project Team Meetings, as required.
- Inventories, coordinates, and tracks timely shipments of clinical study center supplies and drugs to investigational sites, as needed.
- Sorts run and submit requested periodic reports from a computer database, as required.
- Assists and contributes to individual development and training, knowledge, and expertise through research, technical bulletins, and attending appropriate seminars.
- Develops and edits PowerPoint multi-media presentations.
- Organizes and supports teleconferences/videoconferences and internal/external meetings, including coordinates/reserves conference logistics, audiovisual equipment, food arrangements, etc.
- Drafts, edits, and processes correspondence, reports, memos, forms, etc.
- Maintains site master files, source documents, and other site-related activities.
- Should report principal investigator at the site every day for day-to-day activities.
- Adapts to various situations and adjusts to shifting priorities.
- Performs other duties as assigned.
**Salary**: ₹11,000.00 - ₹13,000.00 per month
Schedule:
- Morning shift
**Experience**:
- total work: 1 year (preferred)
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