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The Site Activation Partner I leads and supports operational activities for clinical trials, ensuring compliance with timelines and regulations while managing site activation tasks.

The Clinical Operations Manager oversees trial protocols, manages budgets, ensures compliance with regulations, coordinates teams, and collaborates with vendors for clinical operations.

The Clinical Research Manager oversees project management and compliance for clinical trials, ensuring adherence to regulations and client policies while leading local teams to high performance.

Lead country-level study operations from startup through close for one or more clinical trials. Oversee local study teams and CROs, manage startup, site activation, recruitment strategies, vendor oversight, risk and issue mitigation, and ensure timely delivery of study plans and quality event follow-up.

The Sr. Clinical Research Associate manages and monitors clinical trials, ensuring compliance with regulations, patient safety, and quality delivery at sites.