Job Summary
A company is looking for a Study Start Up Associate II to lead the initiation of clinical trials and ensure compliance with regulatory requirements.
Key Responsibilities
- Lead the preparation and submission of regulatory documents and ethics committee submissions
- Coordinate with internal and external stakeholders to obtain necessary approvals for study initiation
- Manage and maintain accurate records of ethics committee submissions and approvals
Required Qualifications
- Bachelor's degree in life sciences or a related field
- Minimum of 2 years of experience in clinical research, specifically in study start-up activities
- Strong understanding of regulatory requirements and guidelines for clinical trials
- Excellent organizational and project management skills
- Ability to collaborate effectively with cross-functional teams
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