Coordinator-Clin Research 1 (Temporary)

Loma Linda • Loma Linda, CA

2d • $30 - $40

About The Position

The Coordinator-Clin Research 1 assists with implementation of clinical trials conducted by Loma Linda University Health under close supervision of Coordinator 2 and the Direct Supervisor. The role trains to support data quality control and toxicity reporting for study patients receiving care at LLUH and ensures protocol-specific requirements are met. The coordinator works with the Supervisor on clinical research and compliance for 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 includes training and development to prepare for further responsibilities and may be assigned to 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 part of a team 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, think critically and independently, and make quick, informed decisions.
• Ability to use computers and software programs necessary for the position and perform basic math functions.
• Ability to distinguish colors and smells as necessary, hear sufficiently for general conversation in person and on the telephone, identify and distinguish work-related sounds, see adequately to read computer screens and written documents, and discern temperature variances through touch.
• International Air Transport Association (IATA) certificate required within 90 days if handling specimens or dry ice, and must be maintained thereafter.

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.
• Current California nursing licensure or Medical Assistant certification, if applicable.

Responsibilities

• Assist in implementing clinical trials conducted by Loma Linda University Health under close supervision.
• 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 regarding clinical research and compliance for investigators, nurses, and related clinical staff.
• Learn to work independently and balance priorities with supervision and training.
• Complete training and development in preparation for further responsibilities.
• Perform other duties as needed.

What This Job Offers

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