UCLA Health

Senior Clinical Research Coordinator - Hematology/Oncology (Torrance)

UCLA Health • $92K — $149K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in clinical research coordination
  • Proven track record with multicenter clinical trials
  • Strong project management skills
  • Ability to prioritize and manage multiple studies
  • Experience in compliance and regulatory requirements
  • Excellent communication and interpersonal skills

Responsibilities

  • Oversee the operational management of clinical trials from design to closeout
  • Implement research activities for various studies, including NIH and industry-sponsored trials
  • Perform project management tasks to meet scheduled goals
  • Ensure accurate and timely completion of study protocols and procedures
  • Supervise and train team members on project-related tasks
  • Collaborate with PIs, departments, and sponsors to ensure compliance and support study administration

Benefits

  • Opportunities for professional development and training
  • Supportive work environment with a focus on teamwork
  • Access to cutting-edge research and clinical practices
  • Potential for career advancement within the organization
  • Flexible work arrangements to promote work-life balance
Full Job Description
The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader 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. Recognize and perform necessary project management tasks and prioritizes work to reach scheduled goals. The Senior Clinical Research Coordinator is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner. This position may supervise and train others on projects as necessary. Work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of compliance, financial, personnel and other related aspects of studies. Annual salary range: $92,988.23 - $149,588.73

About UCLA Health

UCLA Health is a world-renowned academic medical center located in Los Angeles, California. It comprises four hospitals, including Ronald Reagan UCLA Medical Center, and more than 200 primary and specialty care clinics. UCLA Health is affiliated with the David Geffen School of Medicine at UCLA and is consistently ranked among the top hospitals in the United States. The health system employs over 20,000 people and serves as a major center for patient care, medical education, and research.
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