Coordinator-Clin Research 3

Loma Linda • Loma Linda, CA

16h • $33 - $44 • Onsite

About The Position

The Coordinator-Clin Research 3 is the professional level coordinator that oversees and facilitates the implementation and management of clinical trials conducted by Loma Linda University Health. The position serves as a lead, coordinating study recruitment, scheduling of study related assessments, and follow up of patients. Is responsible and trains on data quality control, training research coordinators, and toxicity reporting of study patients treated at LLUH for care. Ensures protocol specific requirements are achieved. Serves as a subject matter expert 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

• Bachelor's Degree required.
• Three years of clinical research experience in a healthcare setting required.
• Knowledge of medical terminology.
• Ability to read and write legibly.
• Ability to speak in English with professional quality.
• Good interpersonal skills.
• Ability to maintain a 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

• Experience may be considered in lieu of degree.
• Five years of clinical research 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

• Oversees and facilitates the implementation and management of clinical trials.
• Coordinates study recruitment, scheduling of study related assessments, and follow up of patients.
• Responsible for and trains on data quality control.
• Trains research coordinators.
• Handles toxicity reporting of study patients treated at LLUH for care.
• Ensures protocol specific requirements are achieved.
• Serves as a subject matter expert 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.

Benefits

• Equal opportunities in all aspects of the employment process.
• Reasonable accommodations for otherwise qualified individuals requesting an accommodation due to a disability.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level