Role Description:

- Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.

- Implement and conduct assigned clinical trials including but not limited to site readiness, patient/study participant recruitment, study and regulatory documentation, provider support, trial administrative support, and data management.

- Collect and maintain study data and required records of clinical trial activity including but not limited to source documentation, case report forms, drug dispensation records, and regulatory forms.

- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.

- Mentor, train, and provide high-level oversight of other clinical research staff including other Clinical Research Coordinators, and Research Assistants, where necessary.

- Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.

- In addition to trial specific responsibilities, support in building and implementing a scalable operations infrastructure at new, regional Profound Research sites as needed.

Qualifications:

- Associate degree or BS / BA in Life Sciences or related discipline.

- 2+ years prior experience as a clinical research coordinator

- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification preferred.

- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens.

- Excellent attention to detail, organization, and communication with varied stakeholders.

Special Considerations:

- Located in San Diego Metropolitan Area.

- Able to travel regionally as required.