Clinical Research Coordinator I​/II

Responsibilities

• Execute the procedures of the research protocol.
• Safeguard the integrity of study data.
• Actively participate in the screening, recruitment, and retention of clinical trial participants.
• Reconcile research billing, payments, and invoices.
• Manage supply and equipment inventory levels.
• Schedule logistics, determine workflows, and secure resources for defined clinical research trials.
• Serve as an initial point of contact for clinical research participants and clinical staff, providing information regarding research procedures, expectations, and inquiries.
• Ensure participants follow the research protocol and alert Principal Investigator of issues.

• Demonstrated ability to work independently and collaborate effectively with physicians, coordinators, sponsors, and multidisciplinary teams.
• Demonstrated ability to manage multiple priorities simultaneously and consistently meet deadlines in a fast‑paced environment.
• Strong verbal and written communication skills with demonstrated attention to detail and sound professional judgment.
• Working knowledge of medical terminology.
• Demonstrated organizational skills and proficiency with Microsoft Office applications, including Word and Excel.
• Demonstrated problem‑solving and conflict‑resolution skills.
• Ability to reliably travel between multiple work sites with dependable transportation.
• Current ACRP or SoCRA Certification or ability to become certified within 6 months of hire.

• ACRP Certification
• SoCRA Certification