Coordinator-Clin Research 1 (Temporary)

Loma Linda University Health • Loma Linda, CA

1d

About The Position

The Coordinator-Clin Research 1 assists with implementing clinical trials conducted by Loma Linda University Health under close supervision of a Coordinator 2 and direct supervisor. The role receives training to support data quality control and toxicity reporting for study patients treated at LLUH, and ensures that protocol-specific requirements are met. The coordinator works with the supervisor on clinical research and compliance involving investigators, nurses, and related clinical staff. With supervision and training, the coordinator learns to work independently and balance priorities as project direction is received. The position provides training and development in preparation for further responsibilities and may be assigned to either an adult or pediatric area. Other duties may be assigned as needed.

Requirements

• Associate's degree required; experience may be considered in lieu of a degree.
• Knowledge of medical terminology.
• Ability to read and write legibly and speak English with professional quality.
• Good interpersonal skills and the ability to maintain confidentiality and ethical integrity.
• Ability to work as a team member and independently with minimal supervision.
• Ability to remain calm and respond courteously under pressure.
• Ability to organize and prioritize workload and manage multiple assignments effectively.
• Ability to accept direction, recall information accurately, pay close attention to detail, and demonstrate critical independent thinking.
• Ability to make quick, informed decisions and be detail-oriented.
• Ability to use computer and software programs necessary to the position and perform basic math functions.
• Sensory abilities necessary for the position, including distinguishing colors and smells as needed; hearing general conversation in person and by telephone and identifying work-related sounds; seeing computer screens and written documents; and discerning temperature variances through touch.

Nice To Haves

• One year of clinical research experience or experience working with patients in a healthcare setting.
• 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) certification.
• Certified Phlebotomy Technician certification.

Responsibilities

• Assist with implementation of clinical trials conducted by Loma Linda University Health.
• Train to support data quality control and toxicity reporting for study patients treated at LLUH.
• Ensure protocol-specific requirements are achieved.
• Work with the supervisor on clinical research and compliance involving investigators, nurses, and related clinical staff.
• Learn to work independently and balance priorities as project direction is received.
• Perform other duties as needed.

What This Job Offers

• Education Level: Associate degree