As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology.
We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose.
Position Summary
CPM3 is responsible for planning, coordinating, and delivering clinical projects within the Clinical Medical Affairs (CMA) organization. The CPM3 will manage projects such as oversight and governance of clinical studies, MDR submissions/maintenance, evidence generation initiatives, and process improvements, ensuring delivery on time, within scope, and budget.
The CPM3 will report to the Senior Manager, Clinical Research Programs and work closely with cross-functional teams, sponsors, and external vendors using Teleflex’s project management tools (e.g., Planview). This person will be working closely with Senior Directors and Senior Leadership.
Responsibilities
* Plan and deliver projects (e.g., governance of clinical studies, MDR submissions, real world evidence generation, process improvements) from initiation to completion using Planview.
* Define project scope, objectives, and timelines in alignment with organizational priorities.
* Coordinate cross-functional teams and serve as the main point of contact for stakeholders and project sponsors.
* Facilitate project meetings, document actions, and follow up with subject matter experts on deliverables.
* Monitor project progress, risks, and issues, escalating and mitigating as required.
* Track budgets and vendor performance, ensuring adherence to contractual and financial requirements.
* Maintain accurate project documentation and updates within PMO governance tools and standards.
* Ensure compliance with GCP, ICH guidelines, and applicable regulatory requirements.
* Support process improvements to enhance efficiency, reporting quality, and project outcomes.
* Present and communicate project updates to leadership during bi-weekly meetings, ensuring visibility of progress, risks, and needs.
Education / Experience Requirements
* Bachelor of Science/Arts degree in business or technical, engineering, or science discipline (clinical background preferred)
* Experience in medical device related field, minimum 3+ years.
* Minimum of 3+ years’ experience in project management
Specialized Skills / Other Requirements
* PMP certification (Project Management Professional) or Diploma in Project Management preferable.
* Requires track record of detailed project management exhibiting comprehensive planning and thorough communication.
* Experience using MS Project, Planview or equivalent tools to schedule and manage development projects (Planview preferable).
* Must be proficient participating in cross-functional teams, as well as coordinating and communicating to multiple stakeholders.
Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.
If you require accommodation and support to apply for a position, please contact us at talent.emea@teleflex.com.
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