A leading pharmaceutical company in Dublin seeks a Patient Engagement Therapeutic Area Manager responsible for executing patient engagement strategies. The role involves engaging with patient organizations, planning programs with healthcare professionals, and managing operations efficiently. Candidates should possess strong project management skills and fluency in English. This position offers opportunities for personal and professional development in a diverse environment. #J-18808-Ljbffr
Choose LocationChoose Location# Patient Engagement Therapeutic Area ManagerREQ-10064279Dec 08, 2025United Kingdom### SummaryThe Patient Engagement Therapeutic Area Manager (PETAL) is responsible for a defined scope in the execution of Patient Engagement strategies and plans. Ensures all aspects of the daily operations run effectively and efficiently, identify and resolve upcoming issues, improve processes, ensure quality deliverables.### About the Role**Key responsibilities but not limited to:*** Enhance engagement with the patient community through a patient-focused mindset* Identify solutions that educate and empower patient organizations to improve patients disease awareness, quality of life and access to therapies* Work with Franchises, HCPs and patient organizations to plan and implement short and long term programs to meet both business and disease communities needs* Stay current with relevant information and resources regarding industry and health care legislation* Provide updates regularly to the disease communities* Monitor metrics and audience statistical analysis and planning* Report technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt* Distribution of marketing samples (where applicable)**Key performance indicators:*** Quality of documents prepared (presentations etc.)* Feedback from internal and external stakeholders* High-quality delivery of individual contribution within projects* Timeliness, reliability and quality of managed tasks**Essential criteria:*** Project management expertise* Operations management and execution**Languages:**English (written**Why Novartis:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:DevelopmentDevelopmentUnited KingdomLondon (The Westworks)GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.Dublin (NOCC), IrelandCommunications & Public AffairsFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10064279### Patient Engagement Therapeutic Area ManagerREQ-10064279### Patient Engagement Therapeutic Area Manager #J-18808-Ljbffr
Choose LocationChoose Location# Director - Pipeline GovernanceREQ-10066076Nov 27, 2025Switzerland### SummaryLocations: Basel, Switzerland; Dublin, Ireland; Westworks, London, UK Full time Hybrid The Director, Pipeline Governance, plays a pivotal role in shaping how development projects are managed and executed across the organization. This position leads to the optimization of portfolio governance and project management processes, ensuring seamless, compliant, and efficient planning for drug development programs. By driving alignment on governance frameworks, standardizing data models, and harmonizing workflows, the Director enables clarity and consistency across functions and units.### About the RoleThe Director Pipeline Governance champions best practices that safeguard data integrity and system reliability while fostering collaboration across functions. With a focus on innovation and operational excellence, the Director spearheads adoption and enhancement of cutting-edge planning capabilities/ systems, deliver training and change management to empower teams. This is an opportunity to influence strategic decisions and create impact by ensuring high-quality, timely, and accurate portfolio data that drives smarter, faster development outcomes. Join us and lead the transformation of governance into a true enabler of success.Key responsibilities:* Drive strategic governance and continuous improvement of project and portfolio management processes and systems to ensure compliance and operational excellence.* Champion best practices that ensure data integrity, process consistency, and system reliability, setting the gold standard for operational performance.* Shape the future of development by aligning and harmonising workflows, data models, and systems to deliver seamless, compliant planning across global teams.* Collaborate with diverse stakeholders to solve complex challenges, implement smart enhancements, and unlock new levels of organisational agility.* Inspire change by leading adoption initiatives, delivering impactful training, and building capabilities that empower teams to thrive in a dynamic environment.Minimum Requirements:* A graduate degree in life sciences (Master’s or equivalent); PhD or similar advanced qualification strongly preferred, with practical understanding of data governance and analytics tools as an advantage.* Proven experience in leading governance and optimization of project and portfolio management processes, with strong familiarity with PPM systems, workflows, and data models.* Track record of driving alignment and standardization across complex, global organizations, ensuring compliance and operational excellence in drug development or related environments.* Evidence of influencing strategic decisions and leading cross-functional initiatives in matrix organizations, building trusted partnerships and delivering results without formal authority.* Influence senior leadership and key decision-makers as a trusted partner, ensuring governance strategies align with bold organisational ambitions.* Drive resource optimisation and proactive risk management, keeping the organisation agile, future-ready, and positioned for success.* Strong capability in change management and adoption of systems, including delivering training and embedding best practices to enhance organizational performance.* Ability to operate under pressure, meeting tight timelines, and engaging confidently with senior stakeholders to shape governance strategies and enable informed decision-making.* Exceptional communication skills demonstrated by tailoring messages for diverse audiences, combined with curiosity and a commitment to continuous improvement and innovation.* Fluent in English (oral and written).**Accessibility and accommodation:** Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:DevelopmentDevelopmentSwitzerlandBasel (City)C028 (FCRS = CH028) Novartis Pharma AGResearch & DevelopmentFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10066076### Director - Pipeline Governance #J-18808-Ljbffr
A leading pharmaceutical company is seeking a Director, Pipeline Governance in Dublin, Ireland. This role is essential in managing and optimizing development projects and processes, ensuring compliance and operational excellence. Candidates should have a graduate degree in life sciences, significant experience in governance, and strong skills in project management, change management, and communication. The position is full-time and hybrid. #J-18808-Ljbffr
Choose LocationChoose Location# Associate Director, Field Capability Development – Spanish SpeakerREQ-10066861Nov 21, 2025Ireland### Summary#LI-Hybrid Location: Dublin, Ireland Relocation Support: This role is based in Dublin, Ireland. Novartis is unable to offer relocation support: please only apply if accessible.### About the Role## **Key Responsibilities*** Lead the design and implementation of commercial and medical excellence programs aligned with business objectives.* Deliver key projects, impactful workshops and training sessions, both in-person and virtually.* Collaborate with cross-functional teams to ensure successful project execution and adoption.* Act as a trusted advisor to senior stakeholders, influencing strategic decisions.* Mentor and develop junior team members to build a high-performing culture.* Manage resources effectively to optimize financial and operational outcomes.* Drive continuous improvement in project management and capability development processes.* Monitor KPIs to ensure delivery of business impact and customer satisfaction.## ## Essential Requirements* Graduate degree in Life Sciences, Pharmacy, Medicine, or related field.* Minimum 10 years’ experience in commercial or medical excellence roles within pharma/healthcare.* Proven leadership in complex projects and cross-functional team environments.* Expertise in capability development and field force excellence strategies.* Strong stakeholder engagement and influencing skills at senior levels.* Experience designing and delivering impactful training and development programs.* Ability to thrive in a matrix and geographically dispersed organization.* Advanced training, coaching and facilitation skills* Full proficiency in English and **Spanish** language skills.# Desirable Requirements* “ Coaching/Coach the Coach” certification.Disclaimer\*: Some restrictions on flexible working options may apply and will be discussed during interview if applicable **Benefits And Rewards** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: **Commitment To Diversity And Inclusion / EEO** Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. **Accessibility And Accommodation** Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion\_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. **Join Our Novartis Network** If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network **Why Novartis:** **Join our Novartis Network:** **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:InternationalMarketingIrelandDublin (NOCC)IE02 (FCRS = IE002) Novartis Ireland LtdMarketingFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10066861### Associate Director, Field Capability Development – Spanish Speaker #J-18808-Ljbffr
Choose LocationChoose Location# Associate Director, Field Capability Development – German NativeREQ-10066859Nov 21, 2025Ireland### Summary#LI-Hybrid Location: Dublin, Ireland Relocation Support: This role is based in Dublin, Ireland. Novartis is unable to offer relocation support: please only apply if accessible.### About the Role## **Key Responsibilities*** Lead the design and implementation of commercial and medical excellence programs aligned with business objectives.* Deliver key projects, impactful workshops and training sessions, both in-person and virtually.* Collaborate with cross-functional teams to ensure successful project execution and adoption.* Act as a trusted advisor to senior stakeholders, influencing strategic decisions.* Mentor and develop junior team members to build a high-performing culture.* Manage resources effectively to optimize financial and operational outcomes.* Drive continuous improvement in project management and capability development processes.* Monitor KPIs to ensure delivery of business impact and customer satisfaction.## ## Essential Requirements* Graduate degree in Life Sciences, Pharmacy, Medicine, or related field.* Minimum 10 years’ experience in commercial or medical excellence roles within pharma/healthcare.* Proven leadership in complex projects and cross-functional team environments.* Expertise in capability development and field force excellence strategies.* Strong stakeholder engagement and influencing skills at senior levels.* Experience designing and delivering impactful training and development programs.* Ability to thrive in a matrix and geographically dispersed organization.* Advanced training, coaching and facilitation skills* Full proficiency in English and **native-level German** language skills.# Desirable Requirements* “ Coaching/Coach the Coach” certification.Disclaimer\*: Some restrictions on flexible working options may apply and will be discussed during interview if applicable **Benefits And Rewards** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: **Commitment To Diversity And Inclusion / EEO** Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. **Accessibility And Accommodation** Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion\_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. **Join Our Novartis Network** If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network **Why Novartis:** **Join our Novartis Network:** **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:InternationalMarketingIrelandDublin (NOCC)IE02 (FCRS = IE002) Novartis Ireland LtdMarketingFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10066859### Associate Director, Field Capability Development – German Native #J-18808-Ljbffr
Choose LocationChoose Location# Associate Director- Lifecycle Management CoEREQ-10059919Nov 17, 2025Ireland### SummaryBusiness Solutions International (BSI) is a newly established team within International CLS with the objective of providing gold standard business solutions to drive excellence in delivery and innovation across the Business Unit. The Consulting and Program Management team within BSI work across International to support and enable delivery of the highest priority programs/projects. One third of International sales will face Loss of Exclusivity (LOE) exposure by end 2026. Our readiness in differentiation from upcoming competition will contribute critically to the success of International. The Lifecycle Management Centre of Excellence (CoE) within the In-Market Brands in International drives value before and after LOE by preparing regions and countries for LOE readiness. They maximize patient reach and optimize stakeholder value through innovative strategies and tactics, ensuring competitive edge at generic or biosimilar entry. The Associate Director (AD) will be part of the BSI team and support the Late Lifecycle Management CoE.### About the Role**Locations:****Ireland, Dublin****Czech Republic, Prague #LI Hybrid****Major Accountabilities:****Key Responsibilities*** Collaborate with countries and international functions to identify opportunities for optimizing Loss of Exclusivity (LoE) strategies in priority regions* Capture and share learnings from early LoE countries to support later LoE countries, creating a comprehensive reference case report document* Lead the integration of two existing SharePoint platforms to establish a one-stop platform for all Generic/Biosimilar (Gx/Bs) testing* Additionally, the role will support countries by sharing up-to-date and relevant information (Gx/Bs-Intelligence) through our Lifecycle Management (LCM) Virtual communities. This role is pivotal in building Late Lifecycle capabilities for the In-Market Brands Portfolio, which includes a diverse mix of small and large molecules in priority countries* Coordinate country-specific workshops* Assist in implementing the Worldwide LCM late lifecycle strategy to effectively compete in the post-LOE market with biosimilar and generic drug entrants* Anticipate and evaluate the scope, timing, and quality of biosimilar and generic competition* Collaborate to develop strategies for LOE projects and capture valuable learnings**Essential Requirements:*** At least 7 years+ senior level pharmaceutical Value & Asset/ Marketing / Finance/ Development/ BD&L/ IP, and/or Regulatory Affairs* Knowledge and experience in late lifecycle management, innovator & generic business* Knowledge of pharmaceutical business- development/ regulatory process, commercial models, emerging markets, IP rights, legislation, and BD&L* Cross-functional collaboration mindset & strategic thinking* Excellent English communication skills**Desirable Requirements:*** Generic or Biosimilar experience with or in Europe or in a Top INTL country in LACan or APMA* Value and Access experience for an understanding what are levers to sustain originator value e.g., in tenders and how to develop innovative pricing strategies as well as understanding of top market Gx/ BS access models.* Basic understanding of regulatory environment and Gx/ Bs approval rules for top 11 countries* Cross-functional collaboration in strategy development with an advanced business mindset that represents organization, with vision and purpose, and a focus on fundamental healthcare systems thinking**Why Novartis:**https://www.novartis.com/about/strategy/people-and-culture **You’ll receive:** You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards **Commitment to Diversity and Inclusion:** Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. **Join our Novartis Network:** If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:InternationalMarketingIrelandDublin (NOCC)IE02 (FCRS = IE002) Novartis Ireland LtdPrague, Czech RepublicBD&L & Strategic PlanningFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10059919### Associate Director- Lifecycle Management CoE #J-18808-Ljbffr
Choose LocationChoose Location# Clinical Quality Assurance – Program LeadREQ-10040952Sep 04, 2025Spain### SummaryLOCATION: London, UK, Dublin, Rep of Ireland, Barcelona, Spain or Basel, Switzerland ROLE TYPE: Hybrid Working, #LI-Hybrid As an Associate Director level, Clinical Quality Assurance – Program Lead within Clinical Quality Assurance, you will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to patients’ safety, rights and well-being.### About the Role**Key Responsibilities:*** Proactively provide QA leadership to the business strategy for assigned programs/trials by ensuring considerable organization awareness (e.g. Interrelationship of departments and business priorities),* Drive implementation of quality strategy within Global Clinical Team (GCT )/ Clinical Trial Team (CTT) under responsibility* Regularly monitor the implementation of the annual Quality Plan pertaining to the assigned programs/studies* Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that Clinical Trial Process (CTP) are in control* Provide robust and clear quality oversight in the following areas of clinical development: + Support/collaborate with key stakeholders (e.g., Country Development Quality (CDQ), Development Units (DUs), GCT and/or CTT members) to ensure that risks are detected and remediated. + Support core governance for quality incident management for critical and major deviations pertinent to the programs being assigned and ensure timely escalation when required. + Provide Good Clinical Practice (GCP) guidance to day-to-day questions arising from Clinical trials deliverables. + Collaborate with Country Development QA and External Service Providers (ESP) QA to drive initiatives relevant to internal monitoring and outsourced activities Quality oversight. + Support inspections preparation and facilitation in collaboration with other QA groups within Research & Development Quality (RDQ). + Support audits and inspections follow-up activities including Corrective & preventative Actions (CAPA) preparation.* Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.* Active participation in continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability* Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.**Essential Requirements:*** Bachelor’s degree in life science or healthcare field required. Advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/ PharmD/ Masters).* 7 years of involvement in regulated activities (GCP/ Pharmacovigilance (PV)), clinical development and/or QA positions.* Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product* development.* Ability to work independently and in a global/matrix environment.* 3 or more years’ experience in managing projects.* Strong skills in GCP, quality and/or clinical development**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:**Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:**Why Novartis:****Join our Novartis Network:****Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:DevelopmentInnovative MedicinesSpainBarcelona Gran VíaES06 (FCRS = ES006) Novartis Farmacéutica, S.A.Basel (City), SwitzerlandDublin (NOCC), IrelandLondon (The Westworks), United KingdomQualityFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ-10040952### Clinical Quality Assurance – Program Lead #J-18808-Ljbffr
