Clinical Program Manager

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion. Who We’re Looking For: Under the guidance of Clinical Affairs leadership, the Clinical Program Manager (CPM) manages a clinical research portfolio across Laborie's Urology, Gastroenterology, and Maternal and Child Health businesses, with primary focus on Urology. The CPM leads clinical research programs, manages direct reports, and collaborates cross-functionally to generate high-quality evidence that supports patient care and business objectives. The role contributes to evidence strategy, represents Clinical Affairs on product development and cross-functional teams, and helps identify unmet clinical needs through data generation and scientific insight. Additional responsibilities may include oversight of investigator-initiated research, scientific communications, and clinical trial operations, ensuring compliance with SOPs, ICH‑GCP, and applicable regulations. About the Role: Responsibilities described below represent the full scope of activities within the Clinical Program Manager role. Specific assignments and level of hands‑on involvement will vary based on program needs, portfolio complexity, and organizational resourcing, with a strong emphasis on delegation, oversight, and cross‑functional collaboration. People Management Manage and lead a Clinical Research team to share the corporate vision, deliver franchise, functional and team objectives and support the team in their personal development. Ensure appropriate training and onboarding for the Clinical Research group at large and manage distribution of workload to ensure project success. Mentor the team to develop specific short and long‑term objectives and lead problem‑solving and resolution efforts in management of risks and issues. Centralized Operations and Monitoring Oversight Coordinate and oversee monitoring strategies (e.g., centralized, on‑site or risk‑based monitoring) to ensure protocol compliance, data quality, and subject safety. Develop and review centralized operational and monitoring tools and metrics (e.g., enrollment, data quality, deviations, monitoring findings) and escalate risks or issues as appropriate. Partner with internal teams and external vendors/CROs to ensure efficient trial execution, adherence to SOPs, and continuous process improvement. Support inspection readiness through maintenance of compliant documentation, oversight of monitoring deliverables, and participation in audit responses as needed. Program Management, Investigator Initiated Research (IIR) Program, and Projects Analyze data from experiments, clinical trials and publications and support the creation of appropriate device claims and regulatory required clinical documentation (e.g., clinical evaluation reports, clinical study reports, usability engineering files). Develop evidence strategy and clinical study designs in conjunction with cross‑functional stakeholders. Manage and facilitate IIR program. Design and manage real world evidence studies (e.g., health outcomes research and registries). Provide support for technical documentation (e.g., PMS, PMCF, CER, CEP) as needed and support design verification and validation studies. Represent Clinical on new product development teams (or assign a Clinical Affairs team member), contributing to product design reviews, risk management, and clinical strategy planning. Lead development and execution of clinical scientific communications plans aligned with evidence strategy, including abstracts, posters, manuscripts, and clinical content for internal and external use. Oversee preparation, review, and approval of scientific materials to ensure accuracy, consistency, and alignment with regulatory, legal, and compliance requirements. Minimum Qualifications Bachelor's degree in Basic or Life Sciences, Engineering, Health Sciences, Medicine, Nursing or related medical discipline with 8 years relevant experience in Clinical Research. Minimum of 1+ years prior management experience or demonstrated ability to lead and align teams to achieve project milestones. Experience supporting clinical trials in all phases (start‑up, conduct, and closeout) including activities such as protocols, informed consent, case report forms, site management (initiation & training), monitoring, and device accountability, etc. Experience working in field of medical devices and thorough knowledge of ICH/GCP Guidelines, ISO 14155, and FDA regulations and EU MDR, including a basic understanding of regulatory requirements in other countries. Experience contributing to cross‑functional new product development teams throughout the development lifecycle. Demonstrated clinical research leadership in evidence generation strategies. Strong project planning and management, critical thinking, decision making, and problem solving. Experience with statistical methods, interpretation and data collection techniques preferred. Ability and willingness for occasional travel. Preferred Qualifications Experience with interventional urology, urology, gastroenterology, or maternal/child health medical devices. ACRP or SOCRA certification. Experience with scientific communications process and working on investigator‑initiated research programs. Why Laborie Paid time off and paid volunteer time. Medical, Dental, Vision and Flexible Spending Account. Health Savings Account with Company Funded Contributions. 401k Retirement Plan with Company Match. Parental Leave and Adoption Services. Health and Wellness Programs and Events. Awarded 2025 Cigna Healthy Workforce Designation Gold Level. Equal Employment Opportunity Laborie provides equal employment opportunities and non‑discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities. #J-18808-Ljbffr Laborie Medical Technologies Corp