Research Manager, Gynecologic Oncology
Apply NowCompany: UCLA Health
Location: Los Angeles, CA 90011
Description:
Description
The Department of OBGYN is seeking to hire a full time Research Manager to provide supervision and oversite for the gynecologic oncology study team. You will supervise unit operations to ensure compliance with departmental and organizational policies, procedures, and defined internal controls. In this role you will also be responsible for supervising operational management of clinical research / trial / study activities from activation, set up, conduct, through closeout. Overseeing the planning and organizing necessary to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). You will serve as liaison with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service.
Main duties for this role will consist of:
Pay Range: $83,800.00 - $179,400.00
The Department of OBGYN is seeking to hire a full time Research Manager to provide supervision and oversite for the gynecologic oncology study team. You will supervise unit operations to ensure compliance with departmental and organizational policies, procedures, and defined internal controls. In this role you will also be responsible for supervising operational management of clinical research / trial / study activities from activation, set up, conduct, through closeout. Overseeing the planning and organizing necessary to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). You will serve as liaison with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service.
Main duties for this role will consist of:
- Clinical Research Team supervision
- Clinical Research Coordination
- Data and Regulatory Management
- Training and Development
- Service Excellence
- Other Duties as assigned
Pay Range: $83,800.00 - $179,400.00