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Clinical project manager 3

Athlone
Teleflex Medical Euro HQ Athlone
Clinical project manager
€60,000 - €80,000 a year
Posted: 25 October
Offer description

Date: Oct 21, 2025

Location: Athlone, L, IE

Company: Teleflex

About Teleflex Incorporated 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™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit the 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 Director, Clinical Programs & CMA Enterprise Excellence and work closely with cross-functional teams, sponsors, and external vendors using Teleflex’s project management tools (e.g., Planview).

You are someone who gets things done, thrives in a fast-paced environment, and is collaborative and easy to work with. This role focuses on execution, compliance, and continuous improvement to support CMA objectives globally. #LI-UH1 #LI-hybrid


Principal 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)
* Minimum of 5-8 years’ experience in medical device related field.
* Minimum of 5 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. Able to manage project prioritization, scheduling, resource utilization, budgeting, and performance validations.
* Excellent written and oral communication skills.
* Have a flexible mindset, and can-do attitude, able to work in a fast-changing environment with competing priorities.
* Strong organizational skills, attention to detail, and business acumen.

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.

Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.

Teleflex follows a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front. Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. © 2025 Teleflex Incorporated. All rights reserved.

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