Director, Clinical Research Operations

Clinical Operations Management:

• Oversight for traveling clinical staff supporting decentralized operations at events and sites.
• Ensure high-quality protocol execution, participant safety, and adherence to GCP and FDA regulations.
• Oversee clinical workflows at sites and mobile deployments, resolving issues impacting quality, recruitment, or compliance.

People Management:

• Manage, develop, and evaluate all clinical research staff (CRCs, nurses, mobile clinicians, and traveling staff).
• Implement training, competency standards, and performance expectations for all clinical staff.
• Provide input into staffing budgets, resource planning, and clinical support models.

Study Management:

• Monitor enrollment, data quality, documentation practices, and clinical performance metrics.
• Partner with regulatory, medical, data, participant experience, and site operations teams to support successful trial delivery.
• Drive continuous improvement in clinical quality, consistency, and operational efficiency.