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Posted on 18 Nov, 2024
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Research / R&D - Pharma / Medical / Health / Biological Sciences
- Job Role - Clinical Research / Clinical Trails - Associate
- Employment type - Full Time
- Work Mode - In Office
Job Description | Role and Responsibilities
- Coordinate the implementation of clinical protocol & documentation at assigned sites in accordance with GCP, company sponsor SOPs, etc.
- Conduct feasibility studies, preparation & finalization of Confidentiality and Clinical Trial Agreements.
Candidate Profile | Who Can Apply
- Minimum 2 years of monitoring/site management experience is required
- Computer skills including proficiency in use of Microsoft Word, Excel, and PowerPoint
Education
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
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