Clinical Research Coordinator

St. Luke's Health System•Boise, ID

19d

About The Position

The Clinical Research Coordinator supports studies across the Research Department. Therapeutic areas may include pediatric and adult specialties, cystic fibrosis, endocrinology, inpatient research, pulmonology, cardiology, and other areas as department needs evolve. Under general supervision, the coordinator identifies eligible patients for research and ensures research protocols are carried out accurately through assessment, planning, intervention, and evaluation.

Requirements

Bachelor’s degree.
Two years of experience.
Current Basic Life Support (BLS) Provider certification through the American Safety and Health Institute, American Heart Association, or American Red Cross.

Responsibilities

Conduct and document the informed consent process under supervision.
Review clinical records and extract necessary data to determine eligibility and complete data submission through the appropriate mechanism.
Conduct research activities in accordance with study protocols.
Document the research process, adverse event grading, consent process, and patient progress on study in the electronic medical record.
Initiate and submit Serious Adverse Event reports to the study sponsor in collaboration with the physician and principal investigator.
May maintain the clinical trials management system and prepare reports as needed.
May prepare for and conduct study monitor visits and audits.
Serve as a liaison and reference for physicians, investigators, and other staff members with questions about the research process.
Collaborate with the investigator and regulatory staff regarding Institutional Review Board requirements.
Perform other duties and responsibilities as assigned.