Coordinator-Clin Research 3
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Before you apply
SalaryNo pay range posted
LocationLoma Linda, CA, United States
Work modeon-site
SeniorityLead
Experience3+ yrs
Company size10,000+ people
First seenOct 18, 2026 · 2w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's Degree required; experience may be considered in lieu of degree
Three years of clinical research experience in a healthcare setting required
Knowledge of medical terminology
Read and write legibly
Speak in English with professional quality
Good interpersonal skills
Maintain high level of confidentiality and ethical integrity
Team player yet work independently with minimal supervision
Work calmly and respond courteously when under pressure
Organize and prioritize workload; manage multiple assignments effectively
Accept direction
Recall information with accuracy
Pay close attention to detail
Show critical independent thinking; make quick and informed decisions, detail-oriented
Use computer and software programs necessary to the position
Perform basic math functions
Distinguish colors and smells as necessary; hear sufficiently; identify and distinguish various sounds; see adequately to read computer screens and written documents; discern temperature variances through touch
International Air Transport Association (IATA) certificate required within 90 days if handling specimen or dry ice, and maintained thereafter
Five years of clinical research experience preferred
Basic Life Support (BLS) certification preferred if performing patient procedures
Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), or Certified Clinical Research Professional (CCRP) preferred
If active California Nursing license and Medical Assistant, provide current licensure or certification
Certified Phlebotomy Technician certification preferred
About the role
Job Summary: The Coordinator-Clin Research 3 is the professional level coordinator that oversees and facilitates the implementation and management of clinical trials conducted by Loma Linda University Health. The position serves as a lead, coordinating study recruitment, scheduling of study related assessments, and follow up of patients. Is responsible and trains on data quality control, training research coordinators, and toxicity reporting of study patients treated at LLUH for care. Ensures protocol specific requirements are achieved. Serves as a subject matter expert regarding clinical research and compliance for investigators, nurses, and related clinical staff. Works independently and balances priorities upon receipt of project direction. May be assigned to either adult or pediatric area. Performs other duties as needed.
Requirements
Education and Experience: Bachelor’s Degree required. Experience may be considered in lieu of degree. Three years years of clinical research experience in a healthcare setting required, five years preferred.
Knowledge and Skills: Knowledge of medical terminology; read and write legibly; speak in English with professional quality; good interpersonal skills; maintain high level of confidentiality and ethical integrity; team player yet work independently with minimal supervision; work calmly and respond courteously when under pressure; organize and prioritize workload; manage multiple assignments effectively; accept direction; recall information with accuracy; pay close attention to detail; show critical independent thinking; make quick and informed decisions, detail-oriented. Use computer and software programs necessary to the position; perform basic math functions; distinguish colors and smells as necessary; hear sufficiently for general conversation in person and on the telephone; identify and distinguish various sounds associated with the work; see adequately to read computer screens and written documents necessary to position; discern temperature variances through touch.
Licensures and Certifications: Basic life Support (BLS) certification issued by the American Heart Association preferred if performing patient procedures. Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), or Certified Clinical Research Professional (CCRP) preferred. If active California Nursing license and Medical Assistant, provide current licensure or certification. International Air Transport Association (IATA) certificate is required within 90 days, if handling specimen or dry ice, and maintained thereafter. Certified Phlebotomy Technician certification preferred.
About the company
Our mission is to continue the teaching and healing ministry of Jesus Christ. Our core values are compassion, excellence, humility, integrity, justice, teamwork and wholeness.