Job Description
- 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: Fresher in Science Field/ Experienced
Schedule: Day shift
Experience total work: 1 year (Preferred)
Job Type: Full-time
Pay: From ₹8,000.00 per month
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required)
Experience:
- total work: 1 year (Preferred)
Work Location: In person
