Coordinator-Clinical Research 1

Loma Linda University Health • Loma Linda, CA

2d

About The Position

The Coordinator-Clinical Research 1 facilitates the implementation of clinical trials conducted by Loma Linda University Health. Is responsible for data quality control and toxicity reporting of study patients treated at LLUH for care. Ensures protocol specific requirements are achieved. Is a resource 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.
• Minimum one year of clinical research or working with patients in a healthcare setting experience preferred.
• Knowledge of medical terminology.
• Ability to read and write legibly.
• Ability to speak in English with professional quality.
• Good interpersonal skills.
• Ability to maintain high level of confidentiality and ethical integrity.
• Ability to work independently with minimal supervision.
• Ability to work calmly and respond courteously when under pressure.
• Ability to organize and prioritize workload.
• Ability to manage multiple assignments effectively.
• Ability to accept direction.
• Ability to recall information with accuracy.
• Ability to pay close attention to detail.
• Ability to show critical independent thinking.
• Ability to make quick and informed decisions.
• Detail-oriented.
• Proficiency with computer and software programs necessary to the position.
• Ability to perform basic math functions.
• Ability to distinguish colors and smells as necessary.
• Ability to hear sufficiently for general conversation in person and on the telephone.
• Ability to identify and distinguish various sounds associated with the work.
• Ability to see adequately to read computer screens and written documents necessary to position.
• Ability to 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 or to be achieved within 1 year of eligibility 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

• Experience may be considered in lieu of degree.
• Active California Nursing license and Medical Assistant certificate preferred.

Responsibilities

• Facilitates the implementation of clinical trials.
• Responsible for data quality control and toxicity reporting of study patients.
• Ensures protocol specific requirements are achieved.
• Serves as a resource 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.

What This Job Offers

• Career Level: Entry Level
• Education Level: Associate degree