Clinical Research Scientist | Leading CRO | Pune

1. Prepare and review study related documents i.e. Protocol, ICD, CRF and related all other documents are part of regulatory submission.
2. Knowledge of the pharmaceutical industry, terminology, and practices.
3. Performing Project Coordination, Project Planning and its Execution and Management.

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

Qualifications

• Any Graduate - Any Specialization
• Any Post Graduate - Any Specialization
• Any Doctorate - Any Specialization

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