Senior Clinical Research Coordinator

Irvine Clinical Research•Los Angeles, CA
•$85,000 - $95,000•Onsite

About The Position

Inglewood Clinical Research, a research site specializing in late-phase CNS clinical trials, is seeking a Senior Clinical Research Coordinator with extensive clinical trial experience. The Senior CRC will serve as a primary coordinator for Phase I–III clinical trials in Neurology, Psychiatry, and Cardiometabolic areas. The position requires experience with study start-up, trial execution, adverse event reporting, source creation and documentation, pharmacy and lab operations, and query resolution. The role also requires clinical leadership to support operations and train staff as needed. This is a full-time, in-person position based at the clinic in the Alzheimer’s Orange County building in Irvine. The starting salary is $85,000 per year, with higher compensation negotiable for candidates with a valid nursing license (RN or LVN), infusion skills, study start-up knowledge, and/or experience training other coordinators. The company pays 100% of individual health, dental, and vision insurance costs for eligible full-time employees. Vacation (PTO) accrues at three weeks per year.

Requirements

  • Five or more years of industry-sponsored drug trial experience.
  • Demonstrated ability to work on high-enrolling Phase II/III clinical trials.
  • Attention to detail and ability to handle multiple tasks with precision.
  • Demonstrated ability to work accurately and quickly with CTMS.
  • Professional spoken and written English.

Nice To Haves

  • Valid nursing license (RN or LVN).
  • Skill in infusions.
  • Demonstrated knowledge of study start-up.
  • Experience training other coordinators.

Responsibilities

  • Coordinate the day-to-day clinical operations of clinical research studies.
  • Perform study procedures in accordance with GCP and study protocols.
  • Organize and maintain paper and electronic study data completely and accurately.
  • Work with recruitment and prescreening teams to meet study enrollment goals.
  • Conduct diagnostic, efficacy, and safety assessments as needed.
  • Mentor and lead less experienced coordinators and/or research assistants.
  • Take ownership of team productivity, including enrollment, and quality metrics.
  • Manage study start-up tasks, including vendor communication and qualification.

Benefits

  • The company pays 100% of individual health, dental, and vision insurance costs for eligible full-time employees.
  • Vacation (PTO) accrues at three weeks per year.
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