Coordinator-Clin Research 3. Perinatal Research. 24 hrs/week.
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.
- Read and write legibly.
- Speak in English with professional quality.
- Good interpersonal skills.
- Maintain high level of confidentiality and ethical integrity.
- Team player yet work independently with minimal supervision.
- Work calmly and respond courteously when under pressure.
- Organize and prioritize workload.
- Manage multiple assignments effectively.
- Accept direction.
- 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.
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.
- Serves as a lead, coordinating 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 opportunity employer
- Reasonable accommodations for individuals with disabilities
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
