Clinical Research Coordinator, Full-Time

Community Hospital•Grand Junction, CO

2d•$23 - $35•Onsite

About The Position

Clinical Research Coordinator II Job Description: Location: Grand Junction, Colorado (This is not a remote position. On-site required.) Schedule: Monday- Friday (days), with Occasional weekends/evenings. Position: Open until January 31, 2026

Requirements

Associate’s degree in a health sciences or related field or equivalency (Two years of related work experience can be substituted for one year of education.)
Two (2) years of relevant experience.
Moderate knowledge of Medical Terminology, Human Anatomy, and Biology.
Understanding of Medical Billing and Insurance processes.
ACRP/SOCRA certification must be obtained within six (6) months of eligibility.
Completion of the following training within 30 days of hire: Human Subjects Protection, Good Clinical Practice, HIPAA, Bloodborne Pathogens, Personal Protective Equipment, and IATA.

Responsibilities

Ensure adherence to all regulatory requirements, including Human Subjects Protection, Good Clinical Practice, HIPAA, and other relevant guidelines.
Track, recognize, and report adverse events and protocol deviations per study requirements.
Oversee regulatory tasks, including document preparation, submission, maintenance, and coordination of monitoring, auditing, and study closure visits.
Ensure timely and accurate data submission and resolution of queries in CRF databases to prevent delinquencies.
Support Principal Investigators (PIs) with patient screening, enrollment, medical chart reviews, eligibility assessments, informed consent discussions, and data management.
Coordinate all research subject visits to ensure protocol adherence and facilitate care team meetings as needed.
Serve as a liaison between healthcare teams, participants, and study-related parties to ensure protocol compliance and quality patient care.
Provide clinical trial information to patients, families, and providers, facilitating referrals and maintaining strong communication channels.
Perform research-related procedures, including vital signs, electrocardiograms (ECG/EKG), administering questionnaires, specimen collection/processing, lab kit inventory, investigational drug accountability, and other delegated tasks.
Assist leadership with study start-up and financial activities, including CDA review, feasibility analysis, activation processes, invoicing, reconciliation, and CTMS protocol builds.
Create billing slips, assist with study invoicing, and manage patient stipend disbursements.
Participate in process improvement initiatives, focusing on enhancing the patient research experience while maintaining regulatory compliance.
Represent the department on institutional committees.
Participate in community outreach and internal/external research education initiatives.
Stay current on research regulations and best practices by participating in virtual, online or other self-study type opportunities, then provide education updates to the team.
Offers assistance and guidance to team members
Conduct secondary eligibility checks to verify inclusion/exclusion criteria for potential study subjects.