Senior Clinical Trials Coordinator & Operations Lead

University of California; Torrance (CA); Presencial; USD 93.000 - 150.000; Jornada completa

Descripción de la vacante

The University of California is seeking a Senior Clinical Research Coordinator to oversee the design, setup, conduct, and closeout of clinical studies. This role may supervise staff and liaise with PIs, sponsors, and sites to ensure compliant, timely execution across multicenter trials and investigator-initiated projects.

Ideal candidate has extensive clinical research experience, strong communication and organizational skills, and understanding of FDA processes, budgeting, and regulatory

Formación

• Minimum of 4+ years of experience in a clinical research setting.
• Interpersonal skills to communicate clearly with students, staff, faculty, and collaborators.
• Ability to interact with patients compassionately.
• Prioritize tasks with competing deadlines while following regulations.
• Analytical skills to evaluate protocols and regulatory requirements.
• Detail-oriented to manage a fast-paced workload.
• Organizational skills to maintain regulatory files and deadlines.
• Proficiency in Adobe and Microsoft Office, especially Excel.
• Knowledge of IRBs, reviews, and funding organizations.
• Strong verbal and written communication to explain complex concepts.
• Ability to handle confidential information with discretion.
• Willingness to travel to multiple clinic sites.
• Experience with FDA processes and procedures.
• Budgeting experience for clinical trials.

Conocimientos

Clinical research

Communication

Regulatory knowledge

Project management

IRB coordination

FDA processes

Budgeting

Educación

Bachelor's Degree

Advanced degree

Herramientas

Adobe

Microsoft Office

Excel

Descripción del empleo

The University of California is seeking a Senior Clinical Research Coordinator to oversee the design, setup, conduct, and closeout of clinical studies. This role may supervise staff and liaise with PIs, sponsors, and sites to ensure compliant, timely execution across multicenter trials and investigator-initiated projects.

Ideal candidate has extensive clinical research experience, strong communication and organizational skills, and understanding of FDA processes, budgeting, and regulatory