Clinical Project Lead - Medical Devices & Trials

Laborie; Maple Grove (MN); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Paid time off and paid volunteer time

Medical, Dental, Vision and FSA

Health Savings Account with Company Ff

401k Retirement Plan with CompanyMatch

Parental Leave and Adoption Services

Health and Wellness Programs andEvents

Cigna Healthy Workforce Designation

Job summary

Laborie is seeking a Clinical Project Manager to lead clinical study management for product development and lifecycle activities. You will manage timelines, budgets, vendors, and cross-functional teams to deliver compliant studies across stages from start-up to closeout.

Ideal candidates hold a life sciences degree, 5+ years in project management within medical devices or pharmaceutical contexts, and experience with cross-functional product development and regulatory requirements such as GCP.

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 produce 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 s ; 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

Bachelor’s degree in life sciences

Project management

Cross-functional teamwork

Critical thinking

Problem solving

Travel readiness

Education

Bachelor’s degree in life sciences, health sciences, nursing, clinical research, public health, biomedical engineering, or a related discipline

Advanced degree preferred

Job description

Laborie is seeking a Clinical Project Manager to lead clinical study management for product development and lifecycle activities. You will manage timelines, budgets, vendors, and cross-functional teams to deliver compliant studies across stages from start-up to closeout.

Ideal candidates hold a life sciences degree, 5+ years in project management within medical devices or pharmaceutical contexts, and experience with cross-functional product development and regulatory requirements such as GCP.