Full job description
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.
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- Assistance in patient selection and recruitment
- Assistance in Informed Consent Process
Job Type: Full-time
Qualification: Fresher in Science Field
Schedule: Day shift
Experience total work: 1 year (Preferred)
Job Type: Full-time
Schedule:
- Morning shift
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required)
Experience:
- total work: 1 year (Preferred)
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From below link, you can join our Telegram Channel – Click Here to Join our Telegram Group
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Follow us on Instagram for Private and Govt Job Updates – Click Here to Follow
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From below link, you can join our Telegram Channel – Click Here to Join our Telegram Group
