Coordinate project plans, manage clinical trial activities, assist with regulatory requirements, and develop study protocols while collaborating with clinical partners and disseminating findings through presentations and written reports.

Support clinical trials by ensuring psychiatric assessment accuracy, conducting rater interactions, and providing feedback on scoring techniques. Participate in calibration activities and maintain high standards of data reliability throughout the trial...

The specialist will support the ViewPoint reporting software throughout the sales process and implementation, focusing on diverse ultrasound environments like Cardiovascular and Women’s Health. Key duties include providing remote and onsite product training, assisting the sales team with strategies, and ensuring customer success through workflow streamlining.

The Senior CRA will oversee CRO and vendor activities while directly contributing to study start-up and conduct, including site monitoring visits to verify data accuracy, assess patient safety, and ensure regulatory compliance. This role also involves serving as a sponsor liaison, resolving discrepancies, mentoring junior staff, and maintaining audit-ready Trial Master File documentation.