- Location
- Thane, IN
- Work mode
- On-site
- Employment
- Full-time
- Experience
- Mid-level
About the role
Thane, Maharashtra, India Full time R1557317 Job Description Summary Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Cli…
Requirements
- Experience in clinical research monitoring
- Knowledge of regulatory standards and guidelines
- Understanding of clinical study protocols
Skills
- clinical research
- site monitoring
- study protocol compliance
- regulatory standards
- data reporting
- site management
- good clinical practices
- monitoring visits
- clinical trial management
About the company
IQVIA
Posted via Adzuna
How to apply
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