Global Clinical Project Manager: Impactful Device Trials

Laborie Medical Technologies Corp; Minnetonka (MN); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid time off

Medical, Dental, Vision

HSA with company contributions

401k with company match

Parental Leave

Wellness programs

Job summary

Laborie is seeking a Clinical Project Manager (CPM) to lead clinical trial activities for assigned projects, ensuring delivery within time, quality, and budget constraints under GMP/ICH guidelines.

The CPM collaborates with the Clinical Program Manager and vendors, oversees trial startup, TMF readiness, budget tracking, and regulatory compliance, and mentors the Clinical Research Team to deliver high-quality results for patients worldwide.

Qualifications

• Bachelor's degree in Life Sciences; Master’s or Doctoral degree preferred.
• 8+ years of clinical operations experience for CPM; in medical device or CRO industry.
• Minimum 2 years of clinical project management experience at a sponsor or CRO.
• Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN.
• Experience with CER, PMS, PMCF, PSUR medical writing.
• Fluent English, excellent verbal and written communication, MS Office skills.

Responsibilities

• Proactively manage trial level operational aspects of the Clinical Research Team including trial timeline, budget, resources, and vendors.
• Provide updates on trial progress to Clinical Program Manager and CTO, covering vendor selection, project plans, budget and timeline, quality standards, and risk mitigation.
• Lead sponsor study startup process: TMF setup, site/vendor agreements, and budget finalization.
• Ensure robust project plans and SOP-compliant operations per ICH/GCP and regulatory requirements.
• Chair Clinical Research Team meetings and maintain timely TMF filing and documentation.
• Monitor vendor deliverables, address issues, and drive training and quality improvements.
• Review and approve vendor invoices with accounting to ensure timely investigator payments.
• Support TMF filing, maintenance, and archival procedures across trials.

Skills

Clinical project management

Fluent English

Effective communication

Vendor management

Education

Bachelor's degree in Life Sciences

Master's or Doctoral degree preferred

Tools

Microsoft Office

Excel

PowerPoint

Outlook/Teams

Job description

Laborie is seeking a Clinical Project Manager (CPM) to lead clinical trial activities for assigned projects, ensuring delivery within time, quality, and budget constraints under GMP/ICH guidelines.

The CPM collaborates with the Clinical Program Manager and vendors, oversees trial startup, TMF readiness, budget tracking, and regulatory compliance, and mentors the Clinical Research Team to deliver high-quality results for patients worldwide.