Clinical Research Co-ordinator
3 days ago
Maintaining the source documents, CRF's, Investigator Site File and other study related documents according to ICH-GCP guideline
- Completing the eCRF
- Maintenance of Investigational Product according to the specific temperature. Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits.
- Organizing ethics committee meetings
- 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.
- Assistance in patient selection and recruitment
- Assistance in Informed Consent Process
**Job Type**:Full-time
**Qualification**:Pharmacy Fresher
**Schedule**: Day shift
Schedule:
- Morning shift
Ability to commute/relocate:
- Calicut, Kerala: Reliably commute or planning to relocate before starting work (required)
**Experience**:
- total work: 1 year (preferred)
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