Clinical Research Associate, Sponsor Dedicated
$57,500–$226,800 year
On-siteMarysville, Washington, United States
Job Summary
Conduct site monitoring visits including selection, initiation, monitoring, and close-out to ensure studies adhere to protocol, regulations, and Good Clinical Practice. Adapt and track subject recruitment plans, administer protocol training, and evaluate site practices for quality and integrity. Manage study progress by tracking regulatory submissions, enrollment, case report form completion, and data query resolution. Maintain Trial Master File and Investigator's Site File documentation, submit visit reports, and generate follow-up letters. Collaborate with study teams and support site financial management and invoice retrieval where applicable. Requires at least two years of on-site monitoring experience and resides in the United States.
Required Qualifications
- Reside in the same country where the job is located
- Bachelor's Degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Proficiency in use of Microsoft Word, Excel and PowerPoint
- Use of a laptop computer and iPhone and iPad (where applicable)
- Good command of English language
- Organizational and problem-solving skills
- Effective time and financial management skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Desired Qualifications
- Bachelor's Degree Degree in scientific discipline or health care preferred
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