Medical Oncology Ireland jobs in Dublin, County Dublin
- AbbVieDublin, County Dublin
- The Programme Manager Lead is responsible for providing governance, coordination, and execution oversight across assigned projects within CDQ (Commercial…
- View all AbbVie jobs - Dublin jobs - Program Manager jobs in Dublin, County Dublin
- Salary Search: Programme Manager Lead salaries in Dublin, County Dublin
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- MSDLeopardstown, County Dublin
- Red Oak North in Dublin is our commercial Head Office for our Animal Health and Human Health businesses in addition to several global and national support…
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- MSDSwords, County Dublin
- Minimum 3 years experience in Computer Systems Validation (CSV) within a GxP-regulated environment, preferably pharmaceuticals, biotechnology, or medical…
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- IQVIADublin, County Dublin
- Ensure that analytical approaches are scientifically rigorous, fit for purpose, and aligned with the clinical, medical, regulatory, safety, or access decision…
- NovartisDublin, County Dublin
- Including min 5 years of coordinating medical or scientific engagement activities, such as advisory boards, medical congresses (including symposia), standalone…
- AbbVieDublin, County Dublin
- Responsible for implementing and maintaining the effectiveness of the integration of projects and NPI into the AbbVie quality system.
- AbbVieDublin, County Dublin
- Reporting to the Director of Sterility Assurance and Contamination Control, the Associate Director of Quality, Microbial Contamination Control is a pivotal role…
- AbbVieDublin, County Dublin
- The role will ensure compliance with applicable regulatory requirements and help ensure that products manufactured at the site meet Good Manufacturing Practice…
- AbbVieDublin, County Dublin
- Experience in a regulated environment—such as pharmaceutical, medical device, food, healthcare, or another quality-controlled industry—is desirable but not…
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- AbbVieDublin, County Dublin
- The Director, Global Engineering Programs will provide project management, direction and oversight to the Global Engineering Programs department as well as…
- AbbVieDublin, County Dublin
- The Director, Global Engineering Programs will provide project management, direction and oversight to the Global Engineering Programs department as well as…
- AbbVieDublin, County Dublin
- The Demand Planning Manager is responsible for analysing demand patterns, assessing forecast trends, interpreting and actioning key performance indicators , and…
- AbbVieDublin, County Dublin
- This role provides quality leadership in support of due diligence activities at third-party manufacturers (TPMs/CMOs) and contributes as a key member of cross-…
- AbbVieDublin, County Dublin
- You will be a technical problem-solver and champion for quality and operational improvements.
- Lead the MEP Program by delivering criteria set out in Reliability…
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- MSDSwords, County Dublin
- Minimum 3 years engineering experience within pharmaceutical, biotechnology, medical device, or other highly regulated manufacturing environments.
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- Beacon HospitalDublin, County Dublin
- A medical degree and active registration as a medical practitioner, including eligibility for registration with the Irish Medical Council.
Job Post Details
Programme Manager Lead
Job details
Full job description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Programme Manager Lead is responsible for providing governance, coordination, and execution oversight across assigned projects within CDQ (Commercial Distribution Quality). The role establishes and maintains consistent project management practices, supports prioritization and decision-making, and ensures delivery against agreed milestones, scope, and timelines. The position also leads cross-functional collaboration, facilitates stakeholder communication, and oversees assigned projects to support effective execution and alignment with business objectives.
- Leads the CDQ PMO function coordinating project managers and resources to drive function and enterprise-wide project success and ensure cross-functional alignment
- Establish and maintain project governance, prioritization, and reporting processes across assigned cross-functional teams and CDQ Functional Teams.
- Translate PMO and business priorities into clear execution plans, milestones, dependencies, and tracking mechanisms.
- Monitor project progress, risks, issues, actions, and dependencies; escalate blockers, decisions, and resource needs as appropriate.
- Develop and maintain standard templates, tools, dashboards, and metrics to support consistent program management practices.
- Lead and coordinate cross-functional teams to support the execution of complex programs, including planning, implementation, and budget tracking where applicable.
- Ensure timely, clear, and consistent communication to stakeholders, including senior leadership, on program status, risks, decisions, and next steps.
- Support the development and rollout of standard program management processes, training, and ways of working across the organization.
- Facilitate governance forums, communities of practice, and communication channels that enable alignment and knowledge sharing.
- Oversee assigned team members, including workload coordination and support for delivery of their responsibilities.
- Maintain alignment with relevant project standards, business requirements, and organizational governance expectations.
- Support continuous improvement of project management processes, tools, and operating rhythms.
Qualifications
- Bachelor’s degree in Science, Engineering, Business, or a related field.
- 10+ years of relevant industry experience, including 5+ years in program or project management.
- Demonstrated experience managing large, complex, cross-functional projects in a pharmaceutical or similarly regulated environment.
- Strong knowledge of GMP manufacturing, supply chain, CMC technical development, and pharmaceutical regulations.
- Proven ability to develop governance models, manage priorities, and drive execution across multiple stakeholders.
- Strong communication, organization, analytical, presentation, and interpersonal skills.
- Demonstrated ability to resolve conflicts and influence cross-functional teams and technical experts.
- Ability to understand technical aspects of complex systems and contribute to detailed problem-solving discussions.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html