Clinical Research Coordinator

Clinical Research Coordinator

We are seeking a Clinical Research Coordinator to support the day-to-day coordination of clinical research studies at the University. The ideal candidate will manage study activities from start-up through closeout, coordinate participant recruitment and informed consent, collect and manage clinical research data, maintain regulatory documentation, and ensure compliance with study protocols, IRB, and institutional guidelines.

EPIC Proficiency

Associate degree with 2+ years of related experience or a Bachelor's degree in a life science, health science, or related field.

Experience coordinating clinical research studies.

Knowledge of medical terminology, clinical research regulations, and Good Clinical Practice.

Proficiency in MS Office.

Strong organizational, communication, and interpersonal skills.

SOCRA or ACRP certification is preferred.

Coordinate clinical studies from initiation through closeout.

Screen, recruit, consent, and schedule study participants.

Collect and manage patient data, laboratory specimens, and study documentation.

Maintain case report forms (CRFs), study databases, and regulatory files.

Prepare IRB submissions and support regulatory compliance.

Coordinate sponsor monitoring visits, audits, and study meetings.

Track study budgets, billing, and project timelines.

Collaborate closely with Principal Investigators, sponsors, and research teams.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)