Director, Global Real-World Evidence – Health Outcomes Scientist, Oncology

🕒 il y a 18 jours

🌐 États-Unis, Royaume-Uni – Distant

🇺🇸 États-Unis – Télétravail 🇬🇧 Royaume-Uni – Télétravail

🍂 Massachusetts, Pennsylvania – Distant

🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote

💵 $204 000 - $340 000 / an

⏰ Temps Plein

🔴 Expert

👔 Directeur

🦅 Parrain de Visa H1B

Cette entreprise a parrainé des visas H1B par le passé.

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10 000+ employés

🏭 Fabrication

💊 Pharmaceutique

🏥 Santé

Manufacturing • Pharmaceuticals • Healthcare

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Description

• Plan, design, and execute multiple studies for a given asset • Manage study timelines, deliverables, and budgets • Assure quality of deliverables and review/sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters, and manuscripts in adherence to SOPs • Identify resources, references, and analyses to inform scientific design • Advise internal and external experts in support of the asset team • Translate evidence needs into study concepts aligned with strategic objectives • Develop innovative and cost-effective approaches to study development and execution • Maintain knowledge of real-world data resources, partnerships, and public initiatives • Advise on data-source suitability for research questions • Develop understanding of customer needs, clinician needs, HTA requirements, and evidence acceptance • Collaborate with internal teams and participate in best-practice sharing sessions • Build relationships across medical, market access, R&D, and commercial teams • Ensure strategic alignment and cross-functional collaboration • Regularly update key stakeholders and business leaders through periodic reporting • Develop relationships with external thought leaders and ensure appropriate methods and research agendas are applied in accordance with GSK policies

🎯 Exigences

• MSc, or equivalent, in health outcomes, health economics, epidemiology, pharmacy, health or life sciences • 3+ years of experience working in the pharmaceutical industry, preferably in a multi-national company • Experience in Oncology or Hematology • Experience planning and delivering individual projects, managing budgets and working within a matrix setting • History of designing RWE studies, including prospective observational studies, cross-sectional and retrospective cohort studies, chart reviews, and database analyses • Proficiency utilizing evidence for HTA submissions, reimbursement and/or medical engagements • Track record of delivering robust payer evidence and engaging meaningfully with external experts and leaders • Expertise with healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in regional and local markets • Experience communicating technical and complex concepts and results to various audiences to impact decision-making • Preferred: advanced scientific degree, such as PhD, PharmD or equivalent • Preferred: experience in prostate cancer • Preferred: experience in global and country oncology roles • Preferred: launch experience

🏖️ Avantages

• Competitive salary • Annual bonus based on company performance • Healthcare and wellbeing programs • Pension plan membership • Shares and savings programme • Remote or hybrid working model • Health care and other insurance benefits for employee and family • Retirement benefits • Paid holidays • Vacation • Paid caregiver/parental and medical leave • Share-based long-term incentive program eligibility

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