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Senior Director, Pipeline Project Management, Oncology

Stevenage

Job Type

Job Function

Project Management

Location

Stevenage

On-Site or Remote

Job Type

Salary

Competitive salary and benefits

About the Role

*Job description* *Site Name:* UK - Hertfordshire - Stevenage, Upper Providence *Posted Date:* Feb 6 2024 GSK is a place where outstanding people do amazing things. As a science-led global healthcare company, we exist to help people do more, feel better, live longer. Our goal is to be one of the most innovative, best performing, and trusted healthcare companies. In GSK, the Pipeline Project Manager (PPM) will act as the ‘COO’ of the asset and will partner with project leads to help teams plot the best course, then accelerate through complexity and uncertainty with no compromise to quality or safety. The Senior Director PPM can be a project-focused position, a leadership position (leading a group of PPMs), or a combination of both. Pipeline Project Managers compose a community of drug/vaccine development and commercialization experts applying industry-leading project management practices to plan and deliver pipeline projects with industry-leading performance: - Apply a holistic perspective and broad knowledge of drug/vaccine development to help Research and Development teams test ideas and optimize the strategy. - Empower teams to challenge convention, manage uncertainty, and accelerate delivery of critical milestones. - Continuously assess progress and clear the way for uninterrupted focus on the critical path. - Build high-performing teams by cultivating trust and outcomes-focused ways of working. - Share learnings and proven practices across PPM so that we learn and grow as an organization. The PPM can also operate at program level, as when a commercialization team oversees multiple projects under the umbrella of a single program strategy. The Senior Director has demonstrated success managing strategically important, top priority R&D pipeline projects and applies strategic drug development and leadership skills to facilitate successful outcomes for Medicine/Vaccine/Early Development Teams. The Senior Director is seen as a thought leader in project management, promoting and helping to establish best practices for project management. The Senior Director leads through others with direct and/or indirect line management responsibilities for a group of PPMs. *Key Responsibilities:* This is a leadership role that is accountable for delivering multiple oncology projects and people development. - Represent programs and PPM team members as part of TA PPM leadership team (where appropriate), leading and/or contributing to organizational strategy, improvement initiatives, capability development efforts, and talent (line) management for a TA PPM group. - As a visible PM leader, work with other PPM leaders and R&D stakeholders within and across TAs to ensure development of an industry-leading project management capability focused on accelerating pipeline projects. - When directly supporting a project, facilitate and/or contribute to asset strategy and evidence strategy, and lead development of the integrated project plan to ensure feasibility and alignment with TA strategy, prioritization, and pipeline performance objectives. - Own the single integrated plan that builds team commitment to shared goals with schedules and budgets based on clear dependencies and assumptions. - Lead options planning, generate recommendations, alternatives, and tradeoffs to strengthen decision-making and optimize the project strategy. - Leads team preparation for governance decisions and owns schedule, risk, and budget inputs. - Identify opportunities to accelerate by challenging constraints that impact critical path and near-critical path activities. - Orchestrate seamless handoffs with focus on the critical path through proactive project plan monitoring, risk management, and cross-functional management of project issues with timely escalation to leadership as required. - Ensure rigor, consistency, and compliance in established systems to drive timely, high-quality data and reporting in and across projects. - Build trusting relationships with the team and stakeholders to encourage transparency and collaboration. Use strong facilitation skills to lead regular project team meetings and apply consistent best practice for meeting agendas, actions, minutes, and other meeting documentation. - Establish and sustain agreed-upon ways of working for effective team communication, decisions, and conflict resolution. - Actively promote GSK’s Code and values. Seek diverse perspectives, cultivate psychological safety, and ensure that all relevant voices are heard to strengthen outcomes and foster broad commitment. Work on any assignment as directed. *Basic Qualifications* - Master’s Degree or equivalent experience in Lifesciences or Business - Strong experience with Planisware, MS Project, and/or other recognized Project Management tool is required. *Project Management Expertise* - Extensive project management experience in a matrix team environment in pharmaceutical R&D. - Demonstrated expertise in all aspects of project management, based on established PM principles and methods (e.g., PMI/PMBOK). - Extensive experience building and maintaining high-quality project plans, budget and resource forecasts, and project management documentation (key assumptions, risks, etc.). - Expert-level ability to communicate clear, concise view of project status, critical path, and upcoming work to help the team and functions work in concert. - Experience leading and facilitating the identification, visualization, and acceleration of the project’s critical path, including the ability to explain the critical path activities and dependencies to project stakeholders. - Extensive expertise in managing project risks, ensuring that the risks across functions are appropriately identified, measured, managed, and communicated. - Expert proficiency in established PM planning tools. - Extensive experience facilitating and documenting effective project team meetings. - Experience leading or contributing to organizational project management capabilities and PM-related improvement initiatives as needed. *Drug Development Experience* - Experience in early and late oncology drug development and organizational knowledge to validate the operational feasibility, challenge project team assumptions, and prompt subject matter experts to consider the impact of portfolio strategy and external landscape (regulatory, commercial, and competitive). - Extensive experience guiding teams to develop recommendations and options inclusive of benefit, cost, and risk trade-offs to realize the project strategy. - Extensive experience preparing for governance interactions to enable funding, resourcing, and strategic and operational project decisions. - Demonstrated experience in championing data quality. - Experience in delivering projects within budget and ensuring efficient use of resources. *Leadership & Interpersonal Skills* - Knowledge of formal high-performance team concepts and experience leading or partnering with project leaders to establish and sustain a high-performance team environment. - Demonstrated ability to build trust and strengthen collaborative relationships with matrixed team members across teams, sub-teams, and functions. - Demonstrated ability to identify, capture, share, and apply learnings and best-practice across projects. - Demonstrated experience proactively collaborating with a wide variety of project, functional, and leadership stakeholders. - Must posses effective, clear, concise communication skills. - Knowledge of established models for critical thinking, innovation, negotiation, and influencing skills, and experience leading teams in the use of those models to achieve positive outcomes. *Preferred Qualifications* - Project/Program Management Professional (PMP) certificate. - Direct line management experience leading within a global project management function with development and talent management responsibilities. - Experience advancing Antibody Drug Conjugate projects. *LI-GSK *Why Us?* GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only). We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Ukdiversity.recruitment@gsk.com or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive . As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. *Important notice to Employment businesses/ Agencies* GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.

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