What Statistical Modeling Jobs are in Ireland?

**Location:** Homebased in Ireland, no travel / fully remote
**Business Unit:** Clinical FSP, sponsor-dedicated
The **Principal Statistical Programmer** will be responsible for the review of datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. The Senior Statistical Programmer will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
**Why Join IQVIA?**
+ Collaborate with industry leaders on projects at the forefront of clinical innovation
+ Gain exposure to a variety of therapeutic areas, indications, and phases
+ Career development opportunities to grow as we grow, AI‑powered career advancement through our internal talent marketplace, Career Connections
+ Mentorship opportunities across the organisation via Employee Resource Groups
+ Flexible working to assist work-life balance and professional success
+ Join a 2026 Fortune® World's Most Admired Companies - nominated for the FIFTH consecutive year
**Responsibilities**
+ Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content
+ Collaborates with study teams to ensure the quality and accuracy - thus submission readiness - of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml)
+ Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data
+ Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO
+ Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format
+ Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group
+ Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables
+ Collaborates with CR&D staff regarding data analysis requests
+ Performs additional statistical analyses including but not limited to:
o Support responses to regulatory agencies
o Generate integrated summary of safety and efficacy
o Support publications and presentations
o Support planning and reporting of clinical trials via exploratory analyses of available data
**Requirements**
+ BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
+ At least 7 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software
+ In depth understanding of clinical programming and/or statistical programming processes and standards
+ Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills
+ Trained / hands on experience of R Programming
+ Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
+ Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent)
+ Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines
+ Experience working in cross-functional, multicultural and international clinical trial teams
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
**Main Responsibilities and Accountabilities:**
Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
Collaborates with study teams to ensure the quality and accuracy - thus submission readiness - of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.
Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables.
**Additional tasks:**
- Collaborates with CR&D staff regarding data analysis requests.
- Performs additional statistical analyses including but not limited to:
o support responses to regulatory agencies,
o generate integrated summary of safety and efficacy,
o support publications and presentations,
o support planning and reporting of clinical trials via exploratory analyses of available data,
**Position Qualifications and Experience Requirements:**
**Education**
- BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
**Experience**
- At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software.
- Indepth understanding of clinical programming and/or statistical programming processes and standards.
- Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills.
- Good experience in R Programming (Trained/Hands on experience)
-Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM).
- Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent).
- Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines.
- Experience in working in cross-functional, multicultural and international clinical trial teams.
**Why IQVIA**
This role will be dedicated to one of IQVIA's largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies. With IQVIA's FSP business unit, you become a core part of a dynamic team dedicated to reshaping the future of healthcare.
**Additional Benefits:**
+ Home-based remote work opportunities
+ Great work/life balance
+ Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors
+ Cohesive team environment fostering a collaborative approach to study work
+ Variety of therapeutic areas, indications and, study phases
+ Job stability; long-term engagements and development opportunities
+ Career advancement opportunities
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

JR Statistical Programmer II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are currently seeking a Statistical Programmer II to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and real world evidence (RWE) studies. Your expertise will contribute to the accurate interpretation of clinical data, helping to ensure the successful delivery of research projects. What You Will Be Doing: Developing, validating, and maintaining complex statistical programs (primarily SAS, with R or Python as applicable) for data manipulation, analysis, and reporting across clinical trials and real world evidence studies. May help lead a Statistical Programming team to create, validate and generate statistical programs consisting of outputs such as listings, tables, figures, and SDTM/ADaM domains (including mapping specifications) of low to moderate complexity at a minimum. All programs must be developed in accordance with documented procedures and project-specific timelines to generate accurate, complete and consistent outputs. Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses. Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets, including SDTM and ADaM, to meet regulatory standards. Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process. Mentoring junior programmers and assisting in training team members on programming techniques and best practices. Your Profile: Bachelor's degree in statistics, mathematics, computer science, or a related field; advanced degree is a plus. Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming, particularly SAS. Typically = 3 years of experience. Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated. Strong experience working with SDTM/ADaM datasets and standards. Experience supporting real world evidence (RWE) studies is highly desirable. Proficiency in programming languages such as SAS, R, or Python, with experience in clinical data management systems. Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently. Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members. #LI-SA1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply To be considered for this role you will be redirected to our careers page & prompted to create a jobseeker account here. To start the process, click the Continue to Application or Login/Register button below. Benefits: Work From Home

Senior Statistical Programmer - Client Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We're looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward-thinking team. At ICON, you'll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision-making in global healthcare. In this role, you'll take ownership of developing and validating high-quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards. Your expertise will directly support the success of our clinical studies and the advancement of life-changing therapies. What You Will Be Doing Designing, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data. Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights. Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs. Supporting the creation of statistical reports, presentations, and regulatory submission documentation. Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team. Your Profile Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline. Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry. Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis. Exceptional analytical and problem-solving abilities, with meticulous attention to detail. Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply To be considered for this role you will be redirected to our careers page & prompted to create a jobseeker account here. To start the process, click the Continue to Application or Login/Register button below. Benefits: Work From Home

**Job Overview:**
As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients' needs, across complex projects and studies.
This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
**Key Responsibilities:**
- Perform, plan co-ordinate, and implement the following for complex studies:
- The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing
- The programming of analysis datasets (derived datasets) and transfer files for internal and external clients
- The programming quality control checks for the source data and to report the data issues periodically
- Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.
- Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams
- Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
- Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines
- Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables
- Use and promote the use of established standards, SOP and best practices
- Provide training and mentoring to SP team members
**Requirements:**
- Bachelor's Degree in Maths, Computer science, Statistics, or related field
- 7+ years' Statistical Programming experience within the Life Science Industry
- Strong Efficacy experience
- Advanced knowledge of statistics, programming and/or clinical drug development process
- Advanced knowledge of computing applications such as R, SAS, SAS Graph and SAS Macro Language
- Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)
Join IQVIA to see where your skills can take you
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge and innovative, in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance, with a strong focus on a positive well-being
Unleash your potential!
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Requisition number:**
**Job category:** Network Contracting & Pricing
Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global scale. Join us to start **Caring. Connecting. Growing together.**
As a **Senior Financial Consultant, Industry Relations** , you'll play a key role on the pre-deal analytics team, supporting rebate modeling and strategic pricing decisions that drive growth and margin performance. In this role, you'll partner closely with teams across Underwriting, Sales, Rebate Contracting and Client Account Management to evaluate client formularies, forecast rebate opportunities and develop competitive solutions for proposals and complex client opportunities.
You'll act as a subject matter expert in rebate modeling, helping translate complex financial and formulary data into clear business insights. This is a solid opportunity for someone who enjoys solving complex problems, influencing commercial strategy and working across teams to support high-impact decisions in a fast-paced environment.
Careers with Optum offer flexible work arrangements and individuals who live and work in the Republic of Ireland will have the opportunity to split their monthly work hours between our Dublin or Letterkenny office and telecommuting from a home-based office in a hybrid work model.
**What you'll do:**
+ Assess and forecast Pharmaceutical and Medical Drug Rebates for proposed client formulary ranging from $50 million to $3 billion in rebates
+ Perform critical role in the analysis of client formularies to determine client eligibility of rebates with respect to manufacturer contracts
+ Build and estimate rebate guarantee models to assist in the economic analysis of market conditions
+ Incorporate strategies across Underwriting, Sales, Client Account Management, and various cross-functional teams to achieve new client growth and margin retention
+ Identify and provide formulary recommendations to ensure rebates are market competitive to achieve new client growth and margin retention
+ Problem solve creatively utilizing rebate knowledge to formulate rebate strategies that will offer market leading rates
+ Ability to work on large and complex RFPs and identify new strategies to maximize rebates to support market competition
+ Identify alternative pricing options and plan design changes based on economic analyses and trends.
+ Review and complete rebate financial and formulary requirements of RFP questions for Proposal Team
+ Gather, summarize and analyze detailed data. Solid aptitude for technical skills is required
+ Assess the risk of pricing guarantees offered
+ Create best practices to maximize efficiency and process workflow for projects with compressed timelines
+ Evaluate client performance and compare forecasts with actuals
+ Audit forecasting tools for accuracy and troubleshoot variances in modeling
You will be rewarded and recognized for your performance in an environment that will challenge you and give you clear direction on what it takes to succeed in your role, as well as providing development for other roles you may be interested in.
**What you will bring:**
_If you don't meet every single requirement, don't let that hold you back - we're just as excited about potential as we are about qualifications and experience, and you could be exactly who we're looking for._
+ Bachelor's degree in Business, Mathematics, Finance, or equivalent professional experience
+ Proven experience in financial analysis, financial modeling, or underwriting
+ Demonstrated solid proficiency in Microsoft Excel and database querying
+ Demonstrated solid communication skills, both written and verbal
+ Demonstrated solid organizational, multitasking, and follow up skills
**Other useful skills and experience include:**
+ MBA, equivalent graduate degree, CPA, or CFA certification
+ Demonstrated background in healthcare or pharmaceutical environments
+ Demonstrated knowledge of PBM and rebate structures
+ Proven experience in PBM underwriting or healthcare contracting
+ Proven experience in financial consulting or auditing
**What We Offer:**
+ Opportunities for professional development
+ Inclusive and supportive team culture
+ Key benefits: Private health insurance, wellness programs, matching pension contribution, lunch provided by the company, training opportunities, employee donations matching and others
**Please note you must currently be eligible to work and remain indefinitely without any restrictions in the country to which you are making an application. Proof will be required to support your application.**
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
_Diversity creates a healthier atmosphere: Optum is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to gender, civil status, family status, sexual orientation, disability, religion, age, race, and membership of the Traveller community, or any other characteristic protected by law. Optum is a drug-free workplace. © 2026 Optum Services (Ireland) Limited. All rights reserved._
\#BBMEMEA

BIM Modelar Location: Dun Laoghaire, Co. Dublin / Balbriggan Co. Dublin Salary:Negotiable Education:Vocational Training/ Third Level Qualifications Type of Position:Permanent full-time position Experience: 5 + years The Role: CSEA seek civil engineering BIM Modelar to work on a range of Civil & Structural Engineering projects including roads, public realm/streetscape, drainage and utilities and site development works including site development associated with building projects. Who you are: Candidates should be enthusiastic diligent team players who have an excellent knowledge and experience of BIM and AutoCAD. Preference will be given to candidates with a proficiency in Revit or Civil 3D. Ideally candidates will have some experience in the area of Road Geometrical Design, preparation of detail design and tender package drawings. Strong written and verbal communication in English is desirable. What you will do: Civil / Structural BIM Experience Design preliminary layouts (in collaboration with project engineer) Drawing Management (record issues, assign numbering, etc.) Skills: BIM Expereince Civil Engineering Civil Tecnician

At AIB, our values guide how we work and how we support each other. We're looking for someone who puts Customer First, takes initiative and Owns the Outcome, and is always looking for ways to Eliminate Complexity. You'll treat colleagues and customers with fairness and Show Respect, and you'll thrive in a culture built on collaboration where we Be One Team to deliver meaningful impact Role: Model Specialist- Quantitative focussed Location: Dublin, Cork, Galway, or Waterford Hubs Summary of role: Group Internal Audit (GIA) is not your typical audit function. We're on an ambitious journey to create the best function we can for AIB and our people. Through our audit charter, we operate independently as the third line of defence to provide assurance to our stakeholders on the adequacy and effectiveness of AIB and its subsidiaries, governance, risk management and internal control environment. Most importantly, we believe that great people are the key to our success. This is why we work hard to build a team of empowered individuals who are driven to excel through collaboration, inclusion and diversity; embracing the unique strengths and insights everyone brings. We are a group of 90+ professionals operating in Ireland and the UK, who always aim for the highest quality. To get the best from our people we support and embrace flexible working arrangements to provide an empowering environment where people get the job done through managing their own time. GIA is now seeking applications from ambitious professionals who are keen to pursue an opportunity as an audit manager specialising in model risk with a focus on quantitative modelling elements. Key Accountabilities Lead comprehensive audits of risk models, with a particular focus on Internal Ratings-Based (IRB) models, including regulatory capital, probability of default (PD), loss given default (LGD), exposure at default (EAD), credit risk rating systems, stress testing, IFRS9 and other material credit and financial risk models. Maintain and continually develop a deep understanding of IRB regulatory requirements, model risk management frameworks, and evolving supervisory expectations, including ECB, EBA, PRA and CRR requirements applicable to model design, validation, governance, monitoring, and use. Provide robust challenge and independent assurance over the effectiveness of model governance, model development, validation activities, performance monitoring, and regulatory compliance across the model lifecycle. Engage with, and influence, senior stakeholders on internal audit findings, remediation actions, and opportunities to strengthen the control environment and model risk management framework. Build and maintain a strong internal and external network, leveraging industry developments, regulatory insights, and peer practices to drive continuous improvement in audit methodology and model risk coverage. Represent GIA at internal governance forums, model oversight committees, and external engagements, including regulatory meetings and inspections, presenting audit conclusions and insights as required. Produce and oversee clear, comprehensive and evidence-based audit documentation that supports findings and recommendations. Lead, coach, and develop a team of quantitative risk auditors and analysts with varying levels of experience, fostering technical excellence in model risk auditing. Contribute to the development of the Internal Audit strategy and annual audit plan, ensuring appropriate coverage of key model risk areas, including IRB models, model change activity, regulatory developments, and emerging risks. What you Will Bring Please note that the following criteria form the basis of your answers on the application form. Relevant third level or postgraduate qualification in an analytical discipline (e.g. mathematics, statistics, computer science); 5 years+ experience in model development and/or model validation, particularly in relation to credit/financial risk models including those subject to regulatory requirements e.g. Capital Requirement Regulations (CRR); Experience with SAS or SQL programming; Excellent oral and written communication skills; Experience in leading a team of specialists including a focus on growth and improvement combined with a desire to share and contribute to the development of junior auditors; An understanding of regulations relating to internal models e.g. EBA Guidelines on Model Risk, CRR; and A strong track record of interaction and collaboration with an array of stakeholders, preferably including regulatory engagement, at all levels with track record of delivery against multiple competing objectives. Why Work for AIB: We are committed to offering our colleagues choice and flexibility in how we work and live and our hybrid working model enables our people to balance their time between working from home and their designated office, subject to their role, the needs of our customers and business requirements. Some of our benefits include; Market leading Pension Scheme Healthcare Scheme Variable Pay Employee Assistance Programme Family leave options Two volunteer days per year Please click here for further information about AIB's PACT - Our Commitment to You. Key Capabilities As part of the selection process, the successful applicant will be expected to demonstrate the AIB Behaviours and ability in the Behavioural and Technical Capabilities reflected below: Please note that the capabilities will only be asked at interview stage. Depth of technical knowledge - Effectively leverages technical knowledge in area of expertise and partners with others to produce solutions and facilitate improved performance and/or optimal/improved outcomes Communication - Communicates with clarity and precision, presenting complex information in a concise format that is audience appropriate; Business partnerships and consulting - Establishes working relationships with stakeholders in order to establish trust; Performs & Transforms - Leads the delivery of impactful model risk audits while shaping the future direction of model risk assurance; Negotiation & Influence - genuine two-way communication to achieve consensus and progress; and Develops & Empowers - develops talent to meet both their career goals and the organisation's goals - sees talent as a critical organisational imperative. If you are not sure about your suitability based on any aspects of the role advertised, we encourage you to please contact the Recruiter for this role, Nicole Pasquetti, at for a conversation. AIB is an equal opportunities employer, and we pride ourselves on being the first bank in Ireland to receive the Investors in Diversity Gold Standard accreditation from the Irish Centre for Diversity. We are committed to providing reasonable accommodations for applicants and employees. Should you have a reasonable accommodation request please email the Talent Acquisition team at Disclaimer: Unsolicited CV's sent to AIB by Recruitment Agencies will not be accepted for this position. AIB operates a direct sourcing model and where agency assistance is required, the Talent Acquisition team will engage directly with our recruitment partners. Application deadline : 30th July 2026 To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

**Requisition number:**
**Job category:** Network Contracting & Pricing
Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global scale. Join us to start **Caring. Connecting. Growing together.**
As an **Associate Director, Rebate Modeling** , you will support the Optum Rx Industry Relations pre-deal analytics team. This team drives OptumRx's rebate strategy by forecasting and optimizing pharmaceutical and medical rebates across complex client formularies. Partnering with Underwriting, Sales, and Rebate Contracting, you will help support the design of competitive, margin-supportive solutions, and analyze client and competitor formularies. Acting as a rebate SMEs, you will support Request For Proposals (RFPs), translate complex economics into clear executive insights, advise on pricing, and ensure accurate forecasting through data analysis, risk assessment, and continuous process improvement.
Careers with Optum offer flexible work arrangements and individuals who live and work in the Republic of Ireland will have the opportunity to split their monthly work hours between our Dublin or Letterkenny office and telecommuting from a home-based office in a hybrid work model.
**What you will do:**
+ Assess and forecast Pharmaceutical and Medical Drug Rebates for proposed client formulary ranging from $50 million to $3 billion in rebates
+ Perform critical role in the analysis of client formularies to determine client eligibility of rebates with respect to manufacturer contracts
+ Collaborate with Underwriting, Sales, Client Account Management, and various cross-functional teams to achieve new client growth and margin retention
+ Identify and provide formulary recommendations to ensure rebates are market competitive to achieve new client growth and margin retention
+ Analysis of competing PBM formularies and identify new rebate options to ensure OptumRx is providing market competitive rebate pricing in client's formulary and work with Rebate Contracting team to secure new rebates in pharmaceutical manufacturer contracts
+ Strategize and problem solve creatively utilizing industry, competitive, client, and rebate knowledge to formulate rebate strategies that will offer market leading rates
+ Serve as a rebate SME across for Underwriting team
+ Ability to work on large and complex RFPs and identify new strategies to maximize rebates to support market competition
+ Ability to simplify complicated rebate information to Executive Leadership in support of their review and approval of rebate proposals
+ Consult and recommend to clients/consultants alternative pricing options and plan design changes based on economic analyses and trends
+ Gather, summarize and analyze detailed data. Solid aptitude for technical skills is required
+ Assess the risk of pricing guarantees offered
+ Create best practices to maximize efficiency and process workflow for projects with compressed timelines
+ Audit forecasting tools for accuracy and troubleshoot variances in modeling
You will be rewarded and recognized for your performance in an environment that will challenge you and give you clear direction on what it takes to succeed in your role, as well as providing development for other roles you may be interested in.
**What you will bring:**
_If you don't meet every single requirement, don't let that hold you back - we're just as excited about potential as we are about qualifications and experience, and you could be exactly who we're looking for._
+ Bachelor's degree in Business, Mathematics, Finance, or equivalent professional experience
+ Proven experience in financial analysis, financial modeling, or underwriting
+ Demonstrated solid proficiency in Microsoft Excel and database querying
+ Demonstrated solid communication skills, both written and verbal
+ Demonstrated solid organizational, multitasking, and follow up skills
**Other useful skills and experience include:**
+ MBA, equivalent graduate degree, CPA, or CFA certification
+ Demonstrated background in healthcare or pharmaceutical environments
+ Demonstrated knowledge of PBM and rebate structures
+ Proven experience in PBM underwriting or healthcare contracting
+ Proven experience in financial consulting or auditing
**What We Offer:**
+ Opportunities for professional development
+ Inclusive and supportive team culture
+ Key benefits: Private health insurance, wellness programs, matching pension contribution, lunch provided by the company, training opportunities, employee donations matching and others
**Please note you must currently be eligible to work and remain indefinitely without any restrictions in the country to which you are making an application. Proof will be required to support your application.**
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
_Diversity creates a healthier atmosphere: Optum is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to gender, civil status, family status, sexual orientation, disability, religion, age, race, and membership of the Traveller community, or any other characteristic protected by law. Optum is a drug-free workplace. © 2026 Optum Services (Ireland) Limited. All rights reserved._
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