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Principal Clinical Research Associate (Remote)
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Job Description
- Req#: 52436
- True Seniority: You have 5+ years of experience and have mastered the nuances of site management. You are looking for a role where your actual skill set-not just your title-is utilized.
- Medical Device Expertise: You have a proven track record specifically in the Medical Device sector. Experience in Cardiology is a significant advantage.
- Site Management Prowess: You prioritize site health and data integrity over "checking boxes." You excel at managing site volume, patient enrollment, and rigorous long-term monitoring.
- Stability: Your career history reflects commitment and steady growth rather than rapid-fire jumping or title inflation.
- Conduct comprehensive monitoring visits (PSV, SIV, RM, COV) across country
- Manage a high volume of site activities, ensuring adherence to protocols, IDE regulations, and ISO 14155 standards.
- Drive enrollment and oversee long-term patient follow-up for complex device studies.
- Act as a primary liaison for clinical sites, fostering strong investigator relationships.
- Minimum 5+ years of CRA experience (must be at a Senior or Principal level).
- Direct Medical Device monitoring experience is required.
- Cardiology therapeutic experience is highly preferred.
- Experience outside of "Big CRO" environments is preferred; we value versatile talent capable of working independently.
- Ability to travel 60% of the time (approx. 2 weeks/month).
- Must be based in the U.S.; Central Time Zone is a plus to bridge Eastern and Western engagements.
Pay Rate Low: 75 | Pay Rate High: 85
We are seeking a high-level, technically proficient Principal CRA to oversee complex monitoring activities for specialized Medical Device trials.
Job Title: Senior / Principal Clinical Research Associate (Medical Device)
Location: Remote
Term: 12-Month Renewable Contract (Plus Benefits)
Compensation: $75-85/hr
Travel: Approximately 60% (2 weeks per month on-site) The Role
We are seeking a high-level, technically proficient Senior or Principal CRA to oversee complex monitoring activities for specialized Medical Device trials. Unlike high-volume CRO environments, this role requires a "hands-on" expert who possesses the deep clinical intuition and technical skills that only come with years of dedicated field experience.
You will manage site performance across the country, focusing on high-enrollment sites and long-term follow-up monitoring.
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