Coordinator-Clinical Research 1

Loma Linda • Loma Linda, CA

2d • $28 - $38 • Onsite

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.
• Knowledge of medical terminology.
• Ability to read and write legibly.
• Ability to speak in English with professional quality.
• Good interpersonal skills.
• Maintain high level of confidentiality and ethical integrity.
• Ability to work as a team player yet 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.
• 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 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.
• Minimum one year of clinical research or working with patients in a healthcare setting experience preferred.
• Active California Nursing license and Medical Assistant certificate preferred.

Responsibilities

• Facilitates the implementation of clinical trials conducted by Loma Linda University Health.
• Responsible for data quality control and toxicity reporting of study patients treated at LLUH for care.
• 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

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree