Clinical Research Coordinator

Prism Vision Group•Spokane, WA

2d•$27 - $55•Hybrid

About The Position

The Clinical Research Coordinator reports to the Manager of Clinical Research and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Coordinator will perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Clinical Research Coordinator has knowledge of the research studies, rationale, subjects and procedures associated with the studies.

Requirements

Bachelor’s degree preferably in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.
2+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)
Excellent Excel, Word, PowerPoint and reporting skills
Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators
Excellent organizational skills and self-management skills to independently manage work flow
Ability to prioritize
Meticulous attention to detail
Knowledge of medical terminology
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies
Experience using Microsoft Office Suite

Nice To Haves

Certification through either ACRP or SoCRA highly preferred

Responsibilities

Leads recruitment efforts and screens potential patients for eligibility for studies.
Obtains informed consent from patients and conducts study visits for clinical trials
Creates Case Report Forms
Completes assessments on study subjects as per protocol
Documents study assessments
Enters study data into EDC systems
Collects, processes, stores and ships lab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
Assists during Sponsor and FDA audits
Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
Documents adverse events and notifies PI, sponsor and IRB
Assumes test article accountability
Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
Travels to investigator meetings
Participates in weekly meetings with the research team, provides study metrics
Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner.