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.

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.

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.

• 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.

• 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.

• 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…