Collaborate with clients to design scientifically rigorous, and ethically sound clinical trial protocols.

Oversee all aspects of clinical trial operations, including site selection, monitoring, and project coordination.

Develop recruitment strategies to identify and enroll eligible participants meeting study criteria.

Navigate regulatory requirements and obtain necessary approvals from regulatory authorities.

Implement quality management systems to ensure adherence to clinical practice guidelines and regulatory standards.

Ensure data accuracy, completeness, and confidentiality in accordance with regulatory requirements.