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Associate Manager- CRO
iQuanti
Bengaluru / Bangalore
Not Disclosed
1 - 6 Years
Full Time - Permanent
Views:221
Applicants:15
Posted on 14 Apr, 2025
Hybrid
Job Description | Responsibilities
- Prepare and review study related documents i.e. Protocol, ICD, CRF and related all other documents are part of regulatory submission.
- Knowledge of the pharmaceutical industry, terminology, and practices.
- Performing Project Coordination, Project Planning and its Execution and Management.
Overview
- Industry - ADVERTISING / PUBLIC RELATIONS / MARKETING / EVENTS
- Functional Area - Research / R&D - Pharma / Medical / Health / Biological Sciences
- Job Role - Clinical Research / Clinical Trails - Associate
- Employment type - Full Time - Permanent
- Work Mode - Hybrid
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Clinical Research Scientist
Clinical Research
Clinical Data Management
Medical Writing
Clinical Operations
Protocol Designing
