New · posted Oct 31
Artivion · Medical Devices
Clinical Research Associate III
- Kennesaw, GA
- On-site
- Full-time
- Senior & Principal
The role
Site Monitoring & Management
- Independently manage 10–15 investigational sites from start-up through close-out
- Perform all monitoring visits (SIV, IMV, COV) in accordance with the Monitoring Plan
- Ensure compliance with protocol, Monitoring Plan, SOPs, and applicable regulations (ISO 14155, FDA, and local requirements)
- Conduct SDV/SDR, informed consent review, and AE/SAE oversight
- Maintain full ownership of assigned investigator sites, ensuring successful site management and performance
- Build and maintain strong relationships with Principal Investigators and site staff
- Provide training, guidance, and ongoing support to site personnel
- Communicate effectively to manage queries, provide updates, and drive issue resolution
- Ensure data quality, timely query resolution, and site compliance
- Identify risks and support audit and inspection readiness
- Collaborate cross-functionally with Data Management, Clinical, and Project Management teams to support study execution
- Attend Investigator and/or Coordinator meetings
Team Support & Mentorship
- Share expertise and provide guidance to junior CRAs, serving as a resource for questions, problem-solving, and best practices
- Support training initiatives and review work, contributing to team development and consistency across sites
- Provide support to upper management as needed, including contributing to study updates, escalations, and operational decision-making
What you need
- 5+ years of CRA experience
- Strong medical device experience
- Medical device experience, cardiovascular/TEVAR preferred
- Solid understanding of GCP and FDA regulatory requirements
- Ability to work independently and effectively multitask, prioritizing competing activities across multiple sites and study demands
- 50-75% of travel is required for this position.
Where you'll work
Kennesaw, GAOn-siteOpen in Maps (opens in a new tab)
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The context around this role
Live data · October 31, 2026
Career trajectory
Where this role sits in Clinical Research
The general path across 14 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not Artivion's own promotion track.
Career resources on Clinical Research
Skills DNA
What this role leans on
How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct5
- Collaboration and leadership5
- GMP and compliance4
- Investigations and CAPA4
- Documentation and SOPs1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Artivion on Regulatory Jobs
- 9
- Open roles
- 9
- Distinct roles
- 2
- Locations
By discipline
- Clinical4 44%
- Regulatory3 33%
- Quality2 22%
By level
- Senior & Principal4 44%
- Manager2 22%
- Associate & Specialist2 22%
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Clinical Research Associate III at Artivion
Open until filled.