Global Senior Clinical Trials Lead

AtriCure, Inc.

Mason (OH)

On-site

USD 120,000 - 170,000

Full time

4 days ago
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Benefits offered by this job

Medical & Dental beginning day 1 of em
401K plus match
Parental Leave
Volunteer Time off
Pet Insurance
On-site fitness center and cafeteria

Job summary

AtriCure, Inc. is seeking a Senior Clinical Project Manager to drive global clinical study execution from start-up through data reporting. You will partner with sites, CROs and internal teams to ensure milestones are met within budget and regulatory expectations.

The role requires leadership of cross-functional teams, strong knowledge of GCP/ISO standards, and the ability to adapt in a fast-paced medical device environment.

Qualifications

  • Bachelor's degree in the sciences or equivalent experience.
  • Minimum 5 years in project management supporting medical device clinical research.
  • Experience coordinating cross-functional teams and CROs.
  • Solid understanding of GCP, ISO, ICH, and FDA requirements.

Responsibilities

  • Manage day-to-day execution of global clinical studies and programs per plan and budget.
  • Oversee program activities including budget and project planning.
  • Coordinate cross-functional teams and CROs, guiding internal study teams.
  • Monitor study progress, provide updates to internal and external stakeholders.
  • Ensure data integrity, audit readiness, and preparation for publications/submissions.
  • Lead site corrective actions and align activities with regulatory expectations.

Skills

Project management
Budget management
Regulatory compliance
Cross-functional leadership
GCP/ISO knowledge

Education

Bachelor's degree in Science

Job description

AtriCure, Inc. is seeking a Senior Clinical Project Manager to drive global clinical study execution from start-up through data reporting. You will partner with sites, CROs and internal teams to ensure milestones are met within budget and regulatory expectations.

The role requires leadership of cross-functional teams, strong knowledge of GCP/ISO standards, and the ability to adapt in a fast-paced medical device environment.

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