Full Time, Permanent
Mumbai (All Areas)
8-13 years
Perform monitoring visits to verify data, evaluate site performance, manage progress of assigned studies by tracking regulatory submissions, manage study operation plans, and coordinate site initiation and monitoring visits.
Skills
Clinical Research
Clinical Operations
Clinical Trials
Clinical Development
Responsibilities
- Perform monitoring visits to verify data
- Evaluate the performance of site
- Manage the progress of assigned studies by tracking regulatory submissions
- Manage study operation plan
- Coordinate for site initiation and monitoring visits
Job Information
- Role: Clinical research Scientist
- Industry Type: Pharmaceutical & Life Sciences
- Department: Research & Development
- Role Category: Pharmaceutical & Biotechnology
Education
- UG: B.Pharma in any specialization
- PG: M.Pharma in any specialization
Qualifications
- M.Pharma with 8+ years experience in managing clinical trial operations for domestic and international markets, particularly for Phase 1 to 4 trials
- Well versed with GCP and NDCT, 2019 Rules
How to apply
Submit your resume to info@finejobs.in