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Benefits offered by this job
Competitive compensation
Comprehensive benefits
Flexible remote working arrangements
Opportunities for advancement
Job summary
A leading clinical research organization is seeking a Clinical Research Coordinator to manage trials in Oregon. This role requires 2-3 years of experience, a strong understanding of regulatory standards, and the ability to travel extensively. Ideal candidates will join a dynamic startup focused on advancing cardiovascular care, offering competitive compensation and flexible remote work arrangements.
Qualifications
Minimum of 2-3 years of clinical research coordinator experience at the site level.
Experience conducting IDE clinical trials is strongly preferred.
Strong understanding of FDA regulations and ICH-GCP guidelines.
Exceptional communication, organizational, and interpersonal skills.
Ability and willingness to travel up to 75% at times.
Responsibilities
Obtain informed consent from clinical trial participants and manage patient interactions.
Collect and accurately enter patient data into electronic data capture systems.
Manage and maintain all site-level clinical trial documentation.
Communicate and collaborate effectively with clinical site teams and sponsors.
Coordinate scheduling of patient visits and conduct patient follow-ups as necessary.
Ensure compliance with regulatory requirements and study timelines.
Skills
Clinical trial management
Patient interaction
Regulatory compliance
Data entry
Communication skills
Job description
A leading clinical research organization is seeking a Clinical Research Coordinator to manage trials in Oregon. This role requires 2-3 years of experience, a strong understanding of regulatory standards, and the ability to travel extensively. Ideal candidates will join a dynamic startup focused on advancing cardiovascular care, offering competitive compensation and flexible remote work arrangements.