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GSK·Pharma·57 minutes ago
57 minutes agoBe an early applicant

Global Medical Director - Multiple Myeloma, Oncology

Home Worker, United States of AmericaSenior · 10-15 years

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About this role

Position Summary

The Global Medical Affairs Director, Oncology (Multiple Myeloma) role provides strategic global medical affairs leadership for an assigned oncology asset or portfolio. The role holder will set and deliver the long-term disease and medicine strategy, lead integrated global medical plans, and shape external clinical practice to help GSK get Ahead of Disease Together and positively impact patient and population health outcomes in oncology. They will operate in a complex matrix, partnering closely with commercial, clinical development, value & evidence, and country medical teams to drive launch and lifecycle success for oncology assets.

The role is within a team reporting to the Vice President, Global Medical Lead (GML) for the specific asset/portfolio. Strategic accountability for all activities aligned to the asset strategy sits with the GML, with implementation and leadership of designated projects led by the Global Medical Affairs Director.


This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Medical Business Leadership

  • Serve as a key medical business leader for the assigned oncology asset/portfolio, accountable to the Global Medical Lead for strategy and execution.

  • Represent the Chief Patient organisation as a medical business leader, applying deep oncology scientific expertise from early development through lifecycle management to improve patient and population outcomes.

  • Lead/support development of the global disease and asset strategy, integrating scientific, clinical, and market insights to understand unmet needs and guide evidence priorities, communication narratives, product positioning, and evidence generation strategy in oncology.

  • Act as a primary interface with senior internal leaders and external stakeholders (clinical experts, advocacy groups, regulators, payors) to shape disease understanding and treatment paradigms in oncology.

  • Think globally while deeply understanding priority LOC needs via extensive partnership with country medical and cross-functional teams; translate local insights into global plans and deliverables.

  • Lead Global Medical Operational Planning for the asset, ensuring plans are externally-focused, insight-driven and delivered on time and on budget across indications and geographies.

Evidence Generation & Data Strategy

  • Partner across R&D, Real-World Evidence (RWE), Health Outcomes, Global Product Strategy and country teams to identify and prioritize oncology evidence generation needs to close data gaps, support clinical and economic differentiation, and optimize clinical care.

  • Develop scientific questions based on prioritized data gaps and work closely with Data Generation leads to shape Phase 3b/4 and value/evidence plans for the asset.

  • Be accountable for timely review and approval of Phase 3b/4 and value evidence/health outcomes studies within remit, ensuring scientific rigor and strategic alignment.

  • Review investigator-sponsored study proposals (ISS) for strategic alignment and scientific merit in liaison with R&D, Safety, Biostatistics and other experts.

Scientific Communications & Publications

  • Partner with Scientific Communications Leads and Integrated Medical Communications teams to align scientific narratives, publication strategy, and engagement tactics to the global oncology medical strategy.

  • Define key scientific messages and provide oversight for integrated scientific communication plans (congress strategy, medical education, digital engagement, omnichannel content) for the asset.

  • Lead development and communication of newsflow for the asset (e.g., data milestones, congress plans, publication timelines) on a regular basis.

  • Drive excellence in scientific engagement by developing a robust global network of external experts (HCPs, payors, patient representatives, regulators) in oncology and collaborating with LOC Medical teams on advisory activities and initiatives to improve care pathways and outcomes.

  • Provide medical signatory/approval for promotional and non-promotional materials (including congress and digital materials) as required per GSK Written Standards.

Cross-Functional Leadership & Matrix Collaboration

  • Lead complex cross-functional initiatives that support the oncology asset strategy (e.g., launch excellence, lifecycle optimisation, indication expansion, access and reimbursement support), ensuring alignment across global and local teams.

  • Provide thought leadership and strategic direction to anticipate future challenges and opportunities in oncology treatment paradigms and evidence requirements.

  • Act as key partner and delegate to the Global Medical Lead as required, representing the GML in cross-functional forums and governance interactions.

People & Culture

  • Inspire and motivate team members across the matrix organization, fostering collaboration, psychological safety, inclusion and high engagement without direct line management accountability.

  • Act as a mentor to junior medical affairs professionals, supporting development and building future medical business leaders within oncology.

Basic Qualifications
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

  • MD/MBBS/PharmD or PhD in a clinical/scientific discipline relevant to oncology (e.g., medical oncology, haematology, tumour immunology).

  • 5+ years of strong experience in Medical Affairs, including roles in LOC/regional/global settings and hands-on leadership of pre-, peri- and post-launch phases of assets.

  • Experience working with regulatory and clinical development strategies across early and late stages of oncology development.

  • Demonstrated track record leading complex matrix initiatives, managing multiple projects and budgets simultaneously, and influencing senior stakeholders.


Preferred Qualifications
If you have the following characteristics, it would be a plus:

  • Advanced clinical training/board certification in oncology or haematology.

  • Global or above-country leadership experience for oncology assets (e.g., global medical lead, global medical director, therapeutic area lead).

  • Strong interpersonal, verbal and written communication skills in English, with the ability to simplify complex science for diverse audiences. 

  • Experience in driving real-world evidence/HEOR programs and shaping access and reimbursement in oncology.

  • Experience working across multiple regions and major markets (US, EU, Japan, China and Emerging Markets).

Why You?

You will join a global medical team where your clinical and scientific leadership will shape evidence and medical strategy for multiple myeloma. You will gain experience leading cross-functional workstreams, designing evidence generation, and engaging with international external experts. The role is based in the United States. Regular travel will be required to meet colleagues, partners, and external experts.

How to Apply

We would love to hear from you. Please submit your CV and a short cover letter that explains why this role matters to you and how you would contribute. If you need adjustments during the recruitment process to support inclusion, tell us and we will work with you. Apply today to help shape medical strategy and improve outcomes for people living with multiple myeloma.

#LI-GSK


Skills

Cross-Functional Leadership, Digital Fluency, Enterprise Thinking, Launch Excellence, Patient Impact

 

 

The US annual base salary for new hires in this position ranges from $198,000 to $330,000. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In 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 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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com

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.

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 the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

PharmaH1B sponsor likely
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