Associate Director, Pipeline Project Management for BD

At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples lives. GSK fosters a culture ambitious for patients accountable for impact and committed to doing the right thing making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science technology and talent to get ahead of disease together.
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Our approach to R&D

The Associate Director Pipeline Project Management for Business Development provides R&D project management for Business Development opportunities and transactions from early diligence through governance deal execution integration and transition to business as usual (BAU) as well as in cases of separation or reversion. Acting as a strategic partner to Business Development Alliance Management and R&D stakeholders the role drives cross-functional alignment to deliver robust ambitious fit-for-purpose development plans that support timely and informed decision making. This includes leading cross-functional planning governance readiness risk management and integration activities while enabling efficient execution and value realization from BD transactions.

The Associate Director leverages drug development across multiple therapeutic areas and phases of development project management and stakeholder relationship expertise to identify and manage risks challenge assumptions drive alignment on timelines resources and costs and ensure successful transfer of knowledge and accountability into ongoing development teams. Operating within a complex matrix environment the role manages multiple projects of moderate complexity with support contributes to continuous improvement of PPM BD ways of working and helps foster a culture of collaboration agility and operational excellence.

Key Responsibilities:

• Provide R&D project management throughout diligence contracting and integration by identifying critical path activities resource constraints and execution risks ensuring issues are actively managed and escalated to Business Development and to enable timely transition to Business As Usual (BAU).
• Develop integrated cross-functional development plans for Business Development opportunities aligning strategy timelines resources costs assumptions dependencies and key value drivers to support governance and decision making.
• Facilitate cross-functional evaluation of development and integration scenarios by challenging assumptions facilitating trade-off discussions identifying risks and opportunities and recommending mitigation and acceleration strategies to maximize deal value and execution success.
• Liaise with BD colleagues to ensure the appropriate subject matter experts (SMEs)/functional leads are included in diligence and knowledge transfer/integration discussions at the appropriate time to ensure adequate planning pre-deal during contracting and post-deal while also ensuring BD teams remain right sized fit for purpose and agile.
• Support BD as needed in reviewing the contract and ensuring inclusion of information related to tech transfer obligation to support smooth implementation of deals.
• Set expectations and timelines with SMEs and hold them accountable for delivering on their due diligence and knowledgetransfer responsibilities and for adequately transferring knowledge within their line function if team members must transition
• Manage moderately complex R&D integration separation and reversion activities across all therapeutic areas and stages of development
• Drive governance readiness through development of high-quality plans risk assessments and recommendations that support timely decision making and value realization.
• Contribute to continuous improvement of PPM BD processes tools and ways of working while fostering a culture of collaboration agility learning and operational excellence.

Basic Qualifications:

• Bachelors Degree in Life Sciences Business or related field.
• Minimum 7 years of experience in R&D drug/vaccine development or related experience.
• Minimum 3 years of experience in a global project or portfolio management role preferably in the pharmaceutical industry (small molecules biologics and/or vaccines) with experience managing drug development projects across multiple phases of development and therapeutic areas.
• Two or more years of experience utilizing Planisware MS project or similar tools.
• Two or more years of experience assessing risk budgets and resource management.

Preferred Qualifications:

• Advanced degree (PhD or MS in Life Sciences or related field or MBA)
• PMP certification
• Experience working in matrixed cross-functional environment
• Experience with Business Development due diligence and/or Integration/Divestment management.
• Experience in Oncology Respiratory or Infectious Disease PM

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Skills

Communication Cross-Departmental Collaboration Decision Making Financial Acumen Innovation Leadership Project Controls Project Management Project Management Governance Project Planning Project Tracking Risk Management Stakeholder Engagement Stakeholder Management Strategic Leadership

If you are based in Cambridge MA; Waltham MA; Rockville MD; or San Francisco CA the annual base salary for new hires in this position ranges $139425 to $232375. The US salary ranges take into account a number of factors including work location within the US market the candidates skills experience education level and the market rate for the addition this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family) retirement benefits paid holidays vacation and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country the relevant compensation will be discussed during the recruitment process.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

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GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

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