Coordinator-Clin Research 1 (Grant Funded)
About The Position
This position is a temporary grant funded position through 12/31/2026 Job Summary: The Coordinator-Clin Research 1 assists in the implementation of clinical trials conducted by Loma Linda University Health, under close supervision of Coordinator 2 and Direct Supervisor. Will train to be responsible for data quality control and toxicity reporting of study patients treated at LLUH for care. Ensures protocol specific requirements are achieved. Works closely with Supervisor regarding clinical research and compliance for investigators, nurses, and related clinical staff. With supervision and training, learns to work independently and balances priorities upon receipt of project direction. Receives training and development to prepare for further responsibilities. May be assigned to either adult or pediatric area. Performs other duties as needed.
Requirements
- Associate's Degree required. Experience may be considered in lieu of degree.
- 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
Nice To Haves
- One year of clinical research or working with patients in a healthcare setting experience preferred.
- 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.
Responsibilities
- Assists in the implementation of clinical trials
- Responsible for data quality control
- Responsible for toxicity reporting of study patients
- Ensures protocol specific requirements are achieved
- Works closely with Supervisor regarding clinical research and compliance for investigators, nurses, and related clinical staff
- Learns to work independently and balances priorities upon receipt of project direction
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees
