Senior Clinical Research Associate

Manages team members and monitors clinical trials. Organizing project team meetings, carrying out experiments, making observations, tracking results, and analyzing data assuring that all clinical practice and safety standards are met.

Responsibilities:
Maintain study-specific files and documentation, including device accountability (where applicable) and site files.
Assist with documentation preparation to support a clinical study.
Perform site qualification, site initiation, monitoring and study closeout activities of study centers (based across the USA).
Monitoring visits from feasibility through to closeout.
Ensure that Standard submission deadlines are met in a timely and accurate manner and documentation is filed.
Assist with the management of research studies, including study site management.
Involved in preparation of submissions (regulatory, EC, protocol docs).

Requirements:
Life Science Degree.
At least three years of independent monitoring experience.