Clinical Project Manager - Medical Devices & Regulatory Studies

Laborie Medical Technologies Corp.; Maple Grove (MN); On-site; USD 100,000 - 130,000; Full time

Benefits offered by this job

Paid time off and paid volunteer time

Medical, Dental, Vision and Flexible F

Health Savings Account with Company-F,

401k Retirement Plan with CompanyMatch

Parental Leave and Adoption Services

Health and Wellness Programs andEvents

Awarded 2025 Cigna Healthy Workforce D

Health Savings Account with Company-F

Job summary

Laborie Medical Technologies Corp. is seeking a Clinical Project Manager to lead investigations from start-up to closeout, overseeing timelines, budgets, vendors, and risks.

You will coordinate cross-functional study activities and ensure regulatory compliance (GCP) across product development lifecycles. The role requires 5+ years in project management within medical devices or pharma, and travel as needed.

Qualifications

• Bachelor’s degree in life sciences, health sciences, nursing, clinical research, public health, biomedical engineering, or a related discipline.
• 5+ years project management experience or a demonstrated ability to lead and align teams to achieve project milestones.
• Experience working in field of medical devices or pharmaceutical industry and working knowledge of medical device regulations.
• Experience participating on cross-functional product development or product lifecycle management teams.
• Strong project planning and management, critical thinking, decision making, and problem solving.
• Ability to travel as needed.

Responsibilities

• Lead study execution activities from study start-up through study closeout; develop and maintain timelines, project plans, budgets, study metrics, and risk management plans.
• Coordinate study activities across investigators and key stakeholders, monitor study progress, expenditures, and resource utilization; facilitate study meetings and provide regular updates.
• Represent clinical affairs on product development and lifecycle management core team; partner with key stakeholders to define clinical evidence requirements and priorities.
• Provide clinical affairs input into study concepts, research questions, feasibility assessment, and clinical evidence requirements for assigned programs; support evaluation of opportunities for new indications, expanded claims, product enhancements, and geographical market expansion.
• Contribute to clinical study design, protocol development, endpoint selection, and evidence generation plans supporting product development, regulatory objectives, and commercial strategies.
• Support clinical assessments and evidence reviews associated with new product concepts and strategic business initiatives.

Skills

Project management

Cross-functional collaboration

Critical thinking

Decision making

Problem solving

Education

Bachelor’s degree in life sciences

Job description

Laborie Medical Technologies Corp. is seeking a Clinical Project Manager to lead investigations from start-up to closeout, overseeing timelines, budgets, vendors, and risks.

You will coordinate cross-functional study activities and ensure regulatory compliance (GCP) across product development lifecycles. The role requires 5+ years in project management within medical devices or pharma, and travel as needed.