Clinical Research Coordinator - Early Phase Program

UCSF•San Francisco, CA

1d•$38 - $45

About The Position

The Early Phase program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating early and late- stage cancer. Our physician-scientists are also researching and developing new and effective treatments for cancer, including clinical trials. The Early Phase program is seeking a Clinical Research Coordinator with an interest in investigational drugs to have oversight over multiple clinical research projects and support our growing program. The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Phase program. The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies. The CRC will assist in the care of early and late-stage cancer patients while they participate in phase 1 and phase 2 clinical trials. In the role, the CRC will attend clinic appointments, follow test results, and assist in ordering appropriate study-related procedures/tests. The CRC will have the opportunity to learn certain aspects of oncology including but not limited to prevention, early detection, treatment/medication management, and end of life care for cancer patients.

Requirements

Interest in investigational drugs
Ability to execute, manage, and coordinate clinical research protocols
Ability to coordinate administrative, data, and patient scheduling operations
Ability to assist in the care of early and late-stage cancer patients
Ability to attend clinic appointments
Ability to follow test results
Ability to assist in ordering appropriate study-related procedures/tests
Ability to learn aspects of oncology including but not limited to prevention, early detection, treatment/medication management, and end of life care for cancer patients.

Responsibilities

Support the management and coordinating the tasks of single or multiple clinical research studies.
Coordinate study required procedures and treatments for study patients.
Manage and update databases to ensure data integrity.
Act as intermediary between sponsors, research staff, and various UCSF departments.
Ensure compliance with all relevant regulatory agencies.
Assist Clinical Research Manager, Associate Director of Clinical Research Programs and/or PI with research tasks.
Maintain relevant regulatory documents in partnership with the Regulatory department.
Report study progress to investigators.
Participate in any internal and external audits or reviews of study protocols.
Perform other duties as assigned.