Senior Clinical Research Coordinator — Hematology/Oncology

UCLA Health; Torrance (CA); On-site; USD 93,000 - 150,000; Full time

Job summary

UCLA Health in Torrance, CA is seeking a Senior Clinical Research Coordinator to manage end-to-end clinical studies from design to closeout. The role requires leading study activities across NIH and industry trials, collaborating with PIs, sponsors, and sites to ensure compliance, safety, and timeliness.

Ideal candidates have 4+ years in clinical research, strong communication, budgeting, and IRB experience, plus proficiency with Excel and the Microsoft Office suite.

Qualifications

• Minimum of 4+ years of experience in a clinical research setting.
• Strong interpersonal and communication skills for diverse stakeholders.
• Ability to manage priorities and meet deadlines amid interruptions.
• Analytical skills to assess protocols and regulatory requirements.
• Detail-oriented with strong organizational abilities.
• Proficiency with Excel and the Microsoft suite.
• Knowledge of local and external IRBs and research committees.
• Ability to handle confidential information with discretion.
• Willingness to travel to various clinic sites as needed.
• Experience with FDA processes and budgeting for trials.

Responsibilities

• Oversee design, setup, conduct, and closeout of clinical studies.
• Lead implementation of study activities across multiple trials.
• Coordinate with PIs, sponsors, and sites to ensure compliance and timelines.
• Manage budgets and regulatory documentation for trials.
• Train and supervise junior staff on study protocols.
• Ensure patient safety and protocol adherence.

Skills

Clinical research

Budgeting

FDA processes

Data analysis

Attention to detail

Microsoft Excel

Adobe suite

Travel willingness

Regulatory compliance

Communication skills

Education

Bachelor's degree

Tools

Adobe Acrobat

Microsoft Office

Job description

UCLA Health in Torrance, CA is seeking a Senior Clinical Research Coordinator to manage end-to-end clinical studies from design to closeout. The role requires leading study activities across NIH and industry trials, collaborating with PIs, sponsors, and sites to ensure compliance, safety, and timeliness.

Ideal candidates have 4+ years in clinical research, strong communication, budgeting, and IRB experience, plus proficiency with Excel and the Microsoft Office suite.