Coordinator-Clinical Research 2
About The Position
The Coordinator-Clinical Research 2 facilitates the implementation and management of clinical trials conducted by Loma Linda University Health. Is responsible for assisting in the training of research coordinators, data quality control, 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
- Associate's Degree required (Experience may be considered in lieu of degree).
- Minimum three years of clinical research experience in a healthcare setting required.
- Knowledge of medical terminology.
- Ability to read and write legibly.
- Ability to speak 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.
- Basic Life Support (BLS) certification issued by the American Heart Association required if performing patient procedures.
- Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), or Certified Clinical Research Professional (CCRP) required within one year of employment and maintained thereafter.
- International Air Transport Association (IATA) certificate is required within 90 days, if handling specimen or dry ice, and maintained thereafter.
Nice To Haves
- Active California Nursing license preferred.
- Medical Assistant certificate preferred.
Responsibilities
- Facilitates the implementation and management of clinical trials.
- Assists in the training of research coordinators.
- Performs data quality control.
- Handles toxicity reporting of study patients.
- Ensures protocol specific requirements are achieved.
- Serves as a subject matter expert regarding clinical research and compliance.
- Works independently and balances priorities.
- May be assigned to either adult or pediatric area.
- Performs other duties as needed.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
