Senior Clinical Research Coordinator

Irvine Clinical Research • Los Angeles, CA

4d • Onsite

About The Position

Inglewood Clinical Research is seeking a Senior Clinical Research Coordinator for its late-phase CNS clinical research site. The Senior CRC will serve as a primary coordinator on Phase I–III trials in Neurology, Psychiatry, and Cardiometabolic areas, leading day-to-day study operations and supporting study start-up, trial execution, adverse event reporting, source documentation, pharmacy and laboratory operations, and query resolution. The position also includes clinical leadership, mentoring and training staff, and responsibility for team productivity and quality metrics.

This is a full-time, in-person position at the clinic in the Alzheimer’s Orange County building in Irvine. The starting salary is $85,000 per year, with a stated salary range of $85,000–$95,000. Higher compensation may be negotiable for candidates with a valid RN or LVN license, infusion skills, study start-up knowledge, and/or experience training other coordinators.

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.
• Command of 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 in a complete and correct manner.
• Work closely 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.
• Own study start-up tasks, including vendor communication and qualification.
• Support trial execution, adverse event reporting, source creation and documentation, pharmacy and lab operations, and query resolutions.

Benefits

• Company pays 100% of individual health, dental, and vision insurance costs for eligible full-time employees.
• Vacation (PTO) earned at a rate of 3 weeks per year.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed