Clinical Research Coordinator

Axelon Services Corporation

Los Angeles, CA

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JOB DETAILS

SALARY

$50–$60 Per Hour

SKILLS

Academic Background, Best Practices, Clinical Research, Clinical Trial, Federal Laws and Regulations, GCP (Good Clinical Practices), Leadership, Maintain Compliance, Mentoring, National Institutes of Health (NIH), Operational Improvement, Operational Strategy, Operations Research, Organizational Skills, People Management, Problem Solving Skills, Process Improvement, Regulatory Requirements, Regulatory Submissions, Research Skills, Standard Operating Procedures (SOP), Startup, Team Lead/Manager, Team Player

LOCATION

Los Angeles, CA

POSTED

4 days ago

Senior Clinical Research Coordinator
Location: 10920 Wilshire Blvd, Los Angeles, CA 90024
Duration: 12 weeks, possible extension

Position Summary
The Senior Clinical Research Coordinator is responsible for overseeing the day-to-day conduct of clinical research studies while ensuring compliance with sponsor, institutional, and regulatory requirements. This role provides leadership, mentorship, and operational oversight to research staff and supports the successful execution of a diverse portfolio of clinical trials.
Required Qualifications
"Minimum of 3 years of clinical research coordination experience.
"At least 1 year of experience serving in a Senior Clinical Research Coordinator or equivalent leadership role.
"Advanced knowledge of:
oGood Clinical Practice (GCP) guidelines
oFDA regulations
oClinical research regulatory requirements
"Experience mentoring, training, and supervising research staff and new team members.
"Knowledge of regulatory submission processes and workflows.
Key Responsibilities
Study Oversight & Operations
"Provide oversight of daily research activities and study conduct across multiple clinical trials.
"Ensure all study procedures are conducted in compliance with sponsor, institutional, federal, and regulatory requirements.
"Support study start-up, maintenance, and close-out activities.
"Monitor study progress and proactively identify and resolve operational issues.
Team Leadership & Mentorship
"Mentor, train, and supervise research staff and new team members.
"Provide guidance on study procedures, policies, and best practices.
"Foster a collaborative and compliant research environment.
Process Improvement
"Develop, implement, and maintain Standard Operating Procedures (SOPs), workflows, and study manuals.
"Identify opportunities to improve operational efficiency and research quality.
Preferred Qualifications
"Experience supporting a broad range of clinical research studies, including:
oPhase I IV clinical trials
oIndustry-sponsored studies
oInvestigator-initiated studies
oNIH-sponsored research
oInterventional and observational studies
oNon-profit and for-profit sponsored research
"Experience working within an academic medical center environment.
"Familiarity with industry-sponsored clinical trials and sponsor interactions.
Additional Information
"Budget management experience is not required.
"NIH and multicenter trial experience are preferred but not required.
"Candidates with experience in academic medical centers and exposure to diverse clinical trial portfolios are strongly encouraged to apply.

About the Company

Axelon Services Corporation

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