Clinical Research Coordinator - Urology

Uclahealthcareers; Northern, Los Angeles (KY, CA); Hybrid; USD 109,430,000 - 176,079,000; Full time

Job summary

The Clinical Research Coordinator at UCLA Health Careers contributes to the operational management of clinical research activities from design to closeout. The role supports multicenter trials, investigator-initiated studies, and programmatic research under the Clinical Trials Administrator.

You will ensure adherence to study protocols and regulatory requirements, collaborating with the PI, departments, sponsors, and central teams to maintain compliant conduct, financial management, and adequate

Qualifications

• Experience implementing research activities for one or more clinical studies including multicenter trials and investigator-initiated research.
• Ability to plan and organize tasks to meet study deadlines and regulatory requirements.

Responsibilities

• Plan and organize necessary tasks to ensure adherence to the study protocol and applicable regulations (FDA CFR, ICH GCP).
• Collaborate with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, and other entities to support all aspects of studies including compliant conduct and financial management.

Job description

Description

Under the direct supervision of the Clinical Trials Administrator, the Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, setup, conduct, through closeout. The ideal candidate is an experienced professional who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. The Clinical Research Coordinator recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. In this role, you will be responsible for planning and organizing necessary tasks 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 also collaborate 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. Salary offers are determined based on various factors, including but not limited to qualifications, experience, and equity.

Hourly Salary Range: $38.19 - $61.45