Clinical Research Coordinator
3 weeks ago
1. Maintaining the source documents, CRF's, Investigator Site File and other study related documents according to 2 ICH-GCP guideline
2. Completing the eCRF
3. Maintenance of Investigational Product according to the specific temperature. Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits.
4. Organizing ethics committee meetings
5. Completing the review forms and submitting all study related documents to EC Coordinating with the local labs, central labs Assistance in Safety Reporting within the required timelines.
6. Assistance in patient selection and recruitment
7. Assistance in Informed Consent Process
Application Deadline: 29/02/2024
Expected Start Date: 01/03/2024
**Job Types**: Full-time, Permanent, Fresher
Pay: ₹8,000.00 per month
Schedule:
- Monday to Friday
Supplemental pay types:
- Performance bonus
**Experience**:
- total work: 1 year (preferred)
Ability to Commute:
- Kannur, Kerala (required)
Ability to Relocate:
- Kannur, Kerala: Relocate before starting work (required)
Work Location: In person
**Speak with the employer**
+91 8891000510
Application Deadline: 29/02/2024
Expected Start Date: 01/03/2024
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