Associate Director, Regulatory AI Capability Lead
Job Description
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job DescriptionKey Responsibilities
Regulatory Operations & Process Improvement
- Lead business process mapping, analysis, design, and optimization initiatives across CMC Regulatory Affairs, including development, registration, post-approval, and lifecycle management activities.
- Identify operational pain points, process gaps, inefficiencies, and opportunities for simplification or digital enablement in partnership with process owners and subject matter experts.
- Apply structured problem-solving and data-driven approaches to evaluate root causes, assess options, and develop practical and sustainable solutions.
- Facilitate cross-functional workshops and working sessions to define current and future-state processes, clarify roles and decision points, and establish implementation plans.
- Support the development and maintenance of process standards, procedures, governance mechanisms, and operational controls that enable consistent execution across CMC Regulatory Affairs.
- Develop and monitor operational measures and KPIs to evaluate process performance, adoption, and opportunities for continued improvement
- Support portfolio, resource, and operational planning activities as needed, including use of enterprise planning and resource forecasting tools.
Digital Enablement, Data & Systems
- Partner with the CMC Digital Enablement Head, business process owners, IT, and other stakeholders to identify and advance digital opportunities that address meaningful regulatory business needs.
- Translate regulatory operational needs and process requirements into clear business requirements and use cases for digital, automation, data, and technology solutions.
- Lead or support the implementation of digital solutions from business problem definition and requirements development through testing, deployment, adoption, and continuous improvement.
- Establish and monitor success metrics for digital and AI-enabled capabilities including adoption, operational efficiency, quality, user experience, and business value realization.
- Evaluate opportunities to apply workflow automation, analytics, artificial intelligence, and emerging technologies to improve regulatory processes and decision-making.
- Support integration of regulatory processes, data, content, and systems to enable more connected and efficient ways of working.
- Partner with data and system owners to improve data quality, usability, and availability for regulatory operations, analytics, and decision-making.
- Develop dashboards, metrics, and operational insights that increase visibility into performance and enable data-driven decisions.
- Support user acceptance testing, implementation readiness, change management, and adoption of new or enhanced digital capabilities.
Cross-Functional Delivery & Change Leadership
- Lead complex cross-functional initiatives involving CMC Regulatory Affairs, Regulatory Affairs, Technical Development, Quality, Manufacturing, Supply Chain, Strategy & Operations, IT, and other relevant stakeholders.
- Establish clear project objectives, scope, deliverables, roles, dependencies, and implementation plans for assigned initiatives.
- Build alignment among stakeholders with differing priorities and translate complex operational or technical topics into clear business decisions and actions.
- Develop recommendations and decision materials for CMC Regulatory Affairs leadership based on analysis of operational challenges, opportunities, risks, and potential solutions.
- Partner with Regulatory Policy, Intelligence, and Health Authority Strategy colleagues to ensure processes and solutions remain aligned with evolving global regulatory requirements and expectations.
- Drive organizational change initiatives to successfully implement new processes, digital tools, and AI-enabled ways of working, including stakeholder engagement, communications, training, adoption strategies and measurement of expected outcomes.
- Promote effective process management and digital ways of working across CMC Regulatory Affairs by sharing tools, methodologies, lessons learned, and scalable approaches.
Qualifications
- BA/BS/MS/MA/MBA in Life Sciences, Engineering or related field preferred with relevant industry experience
- Experience in regulatory operations, CMC Regulatory Affairs, pharmaceutical development, or a related regulated environment.
- Demonstrated experience leading business process design, mapping, optimization, or operational improvement initiatives.
- Experience translating business needs into requirements and partnering with technology teams to implement digital or system-enabled solutions.
- Experience leading complex, cross-functional initiatives in a global and highly matrixed organization.
- Strong understanding of pharmaceutical regulatory processes and the regulatory lifecycle; experience with CMC regulatory processes strongly preferred.
- Familiarity with regulatory information management, document/content management, workflow, data, analytics, automation, or AI-enabled solutions.
- Experience with relevant enterprise platforms and tools such as Veeva Vault, Planisware, Signavio, Visio, Power BI, or similar technologies is desirable.
- Demonstrated ability to analyze complex problems, structure ambiguous issues, develop recommendations, and drive work through implementation.
- Strong facilitation skills with demonstrated ability to gather subject matter expert input and translate it into clear, practical end-to-end processes and requirements.
- Strong communication and influencing skills with the ability to work effectively across functions and organizational levels.
- Lean, Lean Six Sigma, or other process improvement training or certification is desirable; demonstrated practical application of process improvement methodologies is more important than certification alone.
Equal Employment Opportunity (EEO)
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
- £76k - £96k per annumEstimated...Gilead Sciences seeks an Associate Director to lead business strategy and operational improvements within CMC Regulatory Affairs. The role focuses on process optimization, digital enablement, and cross-functional delivery to enhance regulatory operations and support organizational...Suggested
- £98k - £130k per annumEstimatedJob Description Key Responsibilities Regulatory Operations & Process Improvement Lead business process mapping, analysis, design, and optimization... ...and monitor success metrics for digital and AI-enabled capabilities including adoption, operational efficiency, quality...SuggestedFull-time
$138k - $181.5k per annum
...improve product performance. This person will lead on how we define and measure safety, and... ...sits at the intersection of psychology, AI, product development, and applied research... ...launch-readiness criteria for new features and capabilities, identifying risks and ensuring...Suggested- £65k - £87k per annumEstimated...studies stay on track. You will lead a modern, integrated approach... ...R&D function that blends regulatory rigor with innovation, including... .... ~ Emerging Risk and AI Integration: Develop and maintain... ...protected. ~ Training and Capability: Lead the delivery of the exercise...SuggestedLong-term contractFull-timeOn-siteFlexible hours
- £64k - £82k per annumEstimated...environment? Join our dynamic Nature team as a Associate Ecologist in our UK including Manchester,... .... Here’s what you’ll do: Lead the planning and delivery of ecological... ...continued development of our technical capabilities and encourage the embedding of innovation...SuggestedLong-term contractHybrid workingOn-siteRemoteFlexible hours
$161k - $203.5k per annum
...technologies that ensure environmental safety and regulatory compliance. THE ROLE Terrana Biosciences is... ...agriculture. We are seeking an innovative and strategic Associate Director, Molecular Cloning Technologies to lead the vision, development, and scaling of cloning and...Long-term contract- £59k - £78k per annumEstimated...Associate Director, Supply Chain Company: Cycle Pharmaceuticals Ltd Position Summary: This is a full-time position leading our Supply Chain department, working in our Cambridge office on a... ...Reporting to the Chief Operations and Regulatory Officer, you will work closely...Full-timeHybrid workingOn-site
- £45k - £58k per annumEstimated...seeking a Capture Management Lead to join the Water Strategy & Growth... ...to the Strategy & Growth Director for Water, the role will require... ...’ expertise and enterprise capabilities to deliver value-driven, client... ...technological innovations, including AI and autonomy, to provide...Long-term contractFull-timePart-timeHybrid workingOn-siteRemoteFlexible hours
- £69k - £90k per annumEstimated...renowned venture capital firms and named in both the Forbes AI 50 list of “Most Promising Private AI Companies in... ...Grid, LG and DHL. We are looking for an FP&A Lead to build the financial planning and insight capability needed to support that growth. The opportunity...Long-term contractFull-time
- £50k - £66k per annumEstimated...OGT is a leading global provider of clinical and diagnostic genomic solutions... ...Clinical Evidence and Statistics. The Regulatory and Medical Affairs Directorate is responsible for ensuring that... ...Strong scientific writing and review capabilities Experience designing, managing...
- £50k - £66k per annumEstimated...programs. We are currently seeking a Regional Lead to join our Information Management team.... ...strategy—setting standards, developing capability, and ensuring robust governance across... ..., partnering with Client Service Directors and Market Area Leads to translate complex...Full-timeHybrid workingFlexible hours
- £116k - £152k per annumEstimated...Senior Director, AI Enterprise Process & Innovation Center This opportunity is can be located... ...: you'll actively harness existing capabilities, celebrate and promote reuse, export breakthrough... ...? In this pivotal role, you will lead the reinvention of core processes and embed...Full-timeOn-siteFlexible hours
- £81k - £109k per annumEstimated...looking for a stamp taxes specialist at Associate Director or Director level with corporate focused... ...clients and on challenging projects. • Lead on client projects, providing expert... ...ensure that you are supported by a team of capable and engaged tax colleagues. • Take responsibility...Full-timePart-timeHybrid workingOn-siteFlexible hours
- £50k - £65k per annumEstimated...Role - International Regulatory Affairs Director Duration - 12 months Inside IR35 Location - Central Cambridge, UK/ Remote The International... ...should reflect applicable international requirements. Leads the development, communication and updates of the International...Remote
- £47k - £61k per annumEstimated...Senior regulatory leader needed to shape European strategy for oncology medicines, driving approvals... ...products to secure rapid approvals Lead engagement with EMA and European... ...strategic thinking, influencing, and leadership capabilities Critical thinking on regulatory...
$176.1k - $287.3k per annum
...Build our Future Together We are looking for an Associate Director for our Clinical Pharmacology group. The incumbent will provide strategic... ...advancements of one or more programs and/or aptly address significant regulatory hurdles. Is able to contribute to the overall strategic...£80k - £90k per annum
Company: APPLE TECHNICAL RECRUITMENT (UK) Job Type: Permanent Salary: £80000 - £90000 per annum + competitive benefits packagePermanent- £47k - £61k per annumEstimated...Associate Director Cost Management, Cambridge Permanent | Full-time | Hybrid working About this opportunity We are searching for a chartered... ...opportunities. You will also hold a management position, leading a team comprising chartered, assistant & graduate cost managers...PermanentFull-timeHybrid workingOn-siteFlexible hours
£80k - £90k per annum
Company: APPLE TECHNICAL RECRUITMENT (UK) LIMITED Job Type: Permanent, Full Time Salary: £80000 - £90000/annum competitive benefits packagePermanentFull-time£80k - £85k per annum
Company: ASTUTE PEOPLE Job Type: Permanent, Full Time Salary: £80000 - £85000/annum hybrid, car allowancePermanentFull-timeHybrid working- £61k - £79k per annumEstimated...We deliver tailored solutions that directly address our clients’ key challenges, combining our world-leading project expertise with unrivalled programme delivery capabilities and advisory services. APD delivers services to projects ranging in scale and complexity up to £2...Long-term contractFull-timeHybrid workingRelocation packageSkilled worker visaFlexible hoursNight shift
- £69k - £90k per annumEstimated...teams, clients and stakeholders. You will lead projects and contribute to the design,... ...technical risk, cost, speed, quality and regulatory considerations. ~ Act as a trusted technical... .... ~ Strong project management capability, including requirements gathering, planning...Long-term contractFull-timeRelocation packageFlexible hours
- £85k - £112k per annumEstimated...Working at the intersection of science, data, AI and engineering, the role drives the... ...engineering, API-first architecture, self-service capabilities and a strong internal developer... ...Embed security, privacy, resilience, GxP and regulatory compliance into technology design without...Full-timeOn-siteFlexible hours
- £70k - £91k per annumEstimated...Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster... ...science. By harnessing AI’s powerful capabilities, we can use it to model complex biological... ...diseases. We have built a world-leading drug design engine comprising AI models that...Hybrid workingOn-site1 day/week
$176.1k - $287.3k per annum
...with serious diseases. We are seeking an Associate Director, Clinical Sciences to join our... ...functional environment. In this role, you will lead the design, execution, and scientific interpretation... ...boards, steering committees, DMCs, regulatory authority meetings, and investigator...Hybrid working- £55k - £71k per annumEstimated...Summary of job description: The Associate Director - Process Development is responsible for... ...expectation. Key responsibilities: · Leading the Process Development group at... ...· Thorough understanding of current regulatory requirements and practical experience in...Full-time
- £67k - £87k per annumEstimated...reach patients without delay. Our AI-powered data and imaging... ...management is treated as a core capability, not an afterthought. Data management... .... The role will entail leading user acceptance testing for the... ...of clinical data quality and regulatory standards are essential to the...Long-term contractFull-timeImmediate start
- ...Lanpro is a market leading multi-disciplinary consultancy who specialise in Environment led Planning and Design. We work on projects... ...person’s potential, and we’ll help you reach yours. As an Associate Director, you will take a leadership role in the delivery of Landscape...Full-timePart-timeHybrid workingProbationary periodFlexible hours
- £72k - £94k per annumEstimated...and managed services provider, specializing in worldwide leading Industry sectors such as ICT, AI, Technology, Digital Media, Engineering, Automotive and... ...applications and trends, and have comprehensive capabilities from applications to basic software to chips. Bring comprehensive...Full-timeOn-siteImmediate start
- £55k - £72k per annumEstimated...Account Leaders Arcadis is the world's leading company delivering sustainable design, engineering... ...the Global Industry Area Business Directors and Account Leadership Teams Regional... ...to ensure the business has the capabilities required to deliver future growth. What...Long-term contract
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Regulatory AI Capability Lead. Be the first to apply!
- associate director data science Cambridge, Cambridgeshire
- regulatory affairs associate director Cambridge, Cambridgeshire
- associate director qa Cambridge, Cambridgeshire
- associate director Cambridge, Cambridgeshire
- compliance director Cambridge, Cambridgeshire
- regulatory compliance manager Cambridge, Cambridgeshire
- compliance manager Cambridge, Cambridgeshire
- compliance monitoring manager Cambridge, Cambridgeshire
- regulatory manager Cambridge, Cambridgeshire
- quality and compliance manager Cambridge, Cambridgeshire
