Principal Data Manager I

Key Responsibilities:

• Serve as the main point of contact for data management timelines, deliverables, and technical or procedural issues.
• Review, query, and resolve clinical trial data from multiple sources including medical coding, adverse events, etc.
• Contribute to departmental improvement initiatives, staying current with regulatory requirements and industry best practices.

Core Requirements:

• Requires M.Sc. or B.Sc. in a related field and a minimum of 10 years of experience in clinical trial data management.
• Must have in-depth knowledge of clinical trial data management concepts, processes, and regulatory requirements.
• Demonstrated ability to lead and manage data management activities across multiple projects.

Additional Perks:

• Remote work flexibility in accordance with company policy.
• Supportive and collaborative work environment focused on quality and growth.
• Opportunities for professional development and training.