Medix
Senior Clinical Research Coordinator
Category: Clinical Operations | Regular Full-Time | Onsite
Location: Medford, OR
Pay: $75,000 - $85,000
Overview
We are seeking a Senior Clinical Research Coordinator to lead clinical trial teams and oversee studies from start-up through closeout. This role ensures trials are conducted in compliance with protocols, GCP, ICH guidelines, and company SOPs. The Senior CRC also mentors junior staff, manages daily operations, and serves as a subject matter expert in trial execution.
Key Responsibilities
Lead study teams and coordinate all aspects of assigned clinical trials, including start-up, recruitment, regulatory submissions, scheduling, data entry, query resolution, and closeout.
Train, mentor, and delegate tasks to staff while ensuring compliance with protocols and regulatory requirements.
Oversee patient safety reporting, adverse event documentation, and protocol amendments.
Communicate effectively with sponsors, CROs, vendors, leadership, and participants.
Develop and implement recruitment, risk management, and quality control strategies.
Perform clinical duties within scope (e.g., phlebotomy, drug administration, lab processing).
Ensure proper documentation practices, confidentiality, and adherence to SOPs.
Qualifications
Bachelor's degree + 4 years CRC experience, OR Associate's + 6 years, OR HS/technical degree + 8 years.
CRC certification (ACRP or SOCRA) required within 6 months of hire.
Phlebotomy/IV certification as required by state law.
Strong organizational, communication, leadership, and problem-solving skills.
Ability to manage multiple priorities in a fast-paced environment.