Coordinator-Clin Research 1

Loma Linda University Health • Loma Linda, CA

5d • Onsite

About The Position

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.
• 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 be 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.
• Ability to pay close attention to detail.
• Ability to show critical independent thinking.
• Ability to 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.
• Certified Phlebotomy Technician certification preferred.

Responsibilities

• Assists in the implementation of clinical trials.
• Responsible for data quality control and 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.
• Receives training and development to prepare for further responsibilities.
• 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