Executive Director and TA Head - Specialty
Die ganze Ausschreibung von 1925 GlaxoSmithKline LLC
Das ist der Job
Tell us how your experience aligns with the responsibilities and qualifications listed.
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pPosition Summary /ppThe Global Real-World Evidence Health Outcomes Research Therapy Area Head will be the overall leader of the non-interventional data generation team for the specialty therapy area.
Accountabilities include management and development of a team of leaders and scientists with expertise in real-world evidence and other non-interventional study methods.
This role will ensure that team members engage closely with global medical teams and other matrix stakeholders and partners to plan and design data generation plans (DGPs) for priority assets in the TA, drive disciplined execution of studies and activities, translate results and disseminate data and research findings to all relevant internal and external stakeholders. /ppThe Global Real-World Evidence Health Outcomes Research TA Head Specialty will lead the therapy area team to deliver relevant, innovative, and high impact evidence to meet the needs of external stakeholders such as health care professionals, scientific communities, Health Technology Assessment (HTA) and recommending bodies, patient and advocacy groups and other material stakeholders.
The role will work with senior cross-functional leadership in medical affairs, market access, commercial, LoCs to ensure deliverables from this team are strategically aligned, transparent and timely.
This role will ensure evidence generation projects conducted by this team comply with GSK SOPs and external regulatory and research standards. /ppThis role will bring together and consolidate pre-existing teams and will need a clear vision of how to structure and build these groups for the future.
These responsibilities include some of the following: /plipProvide leadership, management, and development of the therapy area team, including recruitment and capability building, support, and improvement opportunities through best practice sharing to create high performing, quality assured resources which support the business. /p /lilipProvide advice and guidance for best practice in evidence methodologies, including enabling external scientific advice, ensuring appropriate protocol review committee’s advice sought and incorporated. /p /lilipDrive innovation across the TA, inform ideas and options through effective engagement with external experts, HTA agencies, methodology and policy forums, and by leveraging knowledge of the external policy and decision maker environment to enable more efficient evidence development for portfolio assets across the lifecycle (e.g. discovery, launching and life cycle management assets) /p /lilipFacilitate alignment and remove barriers to enable more effective interactions within the complex stakeholder matrix, e.g. clinical, commercial, market access, medical affairs functions. /p /lilipNegotiate with key stakeholders as to what evidence is and is not developed, weighing risks and benefits to optimize reimbursement opportunities. /p /lilipRepresent GSK in external collaborations, engagement and scientific evidence requirements with scientific partners, reimbursement bodies and other decision makers. /p /lilipManage the therapy area team’s budget and resources and appoint asset leads and scientists in alignment with portfolio priorities. /p /lilipEnable appropriate infrastructure to gather and communicate metrics of the impact/value for the therapy area activities which can be communicated to critical audiences internally and externally as required. /p /lilipNavigate diverse cultures and understand dynamics of health care systems at the country level including country wealth, payer decision making processes and priorities. /p /lipbr/br/Basic Qualificationbr/We are seeking professionals with the following required skills and qualifications to help us achieve our goals: /plipPhD, PharmD, MD or equivalent level qualification in a relevant scientific area. /p /lilip8+ years of experience in Health Outcomes or evidence generation leadership position. /p /lilipOther advanced scientific or business degree specialized in Health Outcomes or similar. /p /lilip10 + years of experience in Health Outcomes work or similar. /p /lipbr/Preferred Qualificationbr/If you have the following characteristics, it would be a plus: /plipStrong understanding of regulatory requirements and ethical guidelines for observational research. /p /lilipProven track record of successful team management and leadership. /p /lilipExcellent analytical, communication, and presentation skills. /p /lilipAbility to build and maintain effective collaborations with internal and external stakeholders. /p /lilipStrong organizational and project management skills. /p /lipWorking Patternbr/br/This role is based in the United States and is a hybrid role, combining time in the office and remote work.
We look forward to learning about the impact you can make with us. /pp#LI-GSK /p pPlease visit to learn more about the comprehensive benefits program GSK offers US employees. /ppbWhy GSK? /b /ppbUniting science, technology and talent to get ahead of disease together. /b /ppGSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together.
This includes development of NIS research capability, harnessing new and exciting innovations, optimizing resources in alignment with portfolio priorities and ensure capacity to deliver endorsed evidence generation strategies and plans.
The role presents a unique opportunity to shape something new, setting a high bar in the structuring and future delivery of non-interventional research for the therapy area.
This role will require active engagement with other senior leaders, external thought partners and will need to exert significant influence across a diverse range of stakeholders both internal and external. /ppThis role will provide YOU the opportunity to lead key activities to progress YOUR career.
Specific hybrid arrangements will be discussed during the hiring process.br/br/How to Applybr/br/If you are energized by leading evidence strategy that helps patients access important medicines, please apply.
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. /ppPeople and patients around the world count on the medicines and vaccines we make, so we’re 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. /ppGSK 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. /ppbImportant notice to Employment businesses/ Agencies /b /ppGSK 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. /p
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