A company is looking for a Clinical Study Operations Manager.
Key Responsibilities
Oversee study startup planning, site onboarding, and operational oversight to ensure timely execution of clinical studies
Act as the primary contact for clinical sites, facilitating smooth operations and effective communication
Monitor project progress and maintain compliance with GCP, ICH guidelines, and regulatory standards
Required Qualifications
Experience in clinical project management or clinical operations roles
Strong organizational and project management skills
Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements
Knowledge of decentralized data collection and compliance
A proactive mindset with the ability to anticipate challenges and manage multiple priorities
Operation Manager • Southport, Indiana, United States