Clinical Research Associate (m/f), Gorakhpur in Gorakhpur, Uttar Pradesh

Your tasks:
- Monitors clinical trials by conducting independent visits to clinical centers to verify source data, control restricted inventory
- Conduct on-site training of the research teams in the details of the protocols and the products
- Records data from clinical trials for various Company purposes, including regulatory approvals
- Establishes centers for various clinical trials as they are identified
- Provides in-service training to clinical study site personnel and Company affiliates
- Keeps current on rules and guidelines for conducting clinical trials worldwide
- Confirm accuracy of data and do other functions as required by the particular protocol
- Plans clinical study needs for new projects, including timing
- Writes reports related to regulatory requirements and for the open, peer-reviewed literature
- Handles all organizational details of the protocols
Your skills:
- Highly organized with ability to manage multiple tasks with flexibility as tasks change
- Desire to deliver highest quality of service and work product
- Excellent verbal and written communication
- Professional in all communications and interactions
- Ability to prioritize work and manage time
- Attention to detail and high level of accuracy
Location
Gorakhpur
jobid82282
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