Senior Director, Patient Reported Outcomes

🕒 il y a 26 jours

🇺🇸 États-Unis – Télétravail

💵 $222 000 - $292 000 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

👻 Score fantôme 0%

Ce que ça veut dire : la probabilité que personne ne recrute vraiment pour cette offre.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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BeOne Medicines

Site WebLinkedInTous les Emplois

10 000+ employés

Fondée en 2010

🧬 Biotechnologie

🏥 Santé

💊 Pharmaceutique

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines est une entreprise mondiale d’oncologie dont le siège est en Suisse. Elle découvre et développe des traitements innovants, plus abordables et plus accessibles aux patients atteints de cancer dans le monde entier. Avec un portefeuille couvrant l’hématologie et les tumeurs solides, BeOne accélère le développement de son pipeline diversifié de nouvelles thérapies grâce à ses capacités internes et à ses collaborations. Forte d’une équipe mondiale en croissance de plus de 11 000 collaborateurs présents sur six continents, l’entreprise s’engage à améliorer radicalement l’accès aux médicaments pour un bien plus grand nombre de patients qui en ont besoin.

Description

• Develop and execute integrated evidence-generation strategies demonstrating the humanistic value of BeOne Medicines therapies • Provide enterprise-level PRO leadership across assets, indications, therapeutic areas, regions, and product lifecycles • Ensure PRO evidence needs are represented in integrated evidence plans, medical strategies, clinical development plans, and value and access strategies • Advise senior leaders and governance bodies on evidence priorities, investment trade-offs, methodological options, feasibility, timing, and risk • Oversee PRO real-world evidence, observational research, comparative effectiveness and safety research, burden-of-illness studies, patient preference research, health economic models, indirect treatment comparisons, evidence syntheses, and value communication deliverables • Lead complex evidence-generation programs from concept through results dissemination and project closure • Oversee budgets, forecasts, contracts, vendors, timelines, risks, and resource allocation • Ensure scientific rigor, quality controls, compliance, balanced interpretation, and independent technical review • Serve as senior PRO partner to asset teams, medical and development leadership, access teams, governance committees, and regional stakeholders • Translate complex scientific and economic evidence into recommendations for executive, clinical, payer, regulatory, and nontechnical audiences • Contribute to business development, due diligence, portfolio assessment, and external partnership evaluations • Lead or oversee publication and scientific communication strategies • Represent BeOne Medicines at scientific congresses, professional associations, advisory forums, and external engagements • Build relationships with researchers, clinicians, payers, health economists, patient organizations, and external experts • Lead, coach, and develop direct reports and provide matrix leadership to cross-functional colleagues and external teams • Assess capability and capacity needs and recommend hiring, external support, training, tools, standards, and operating-model improvements

🎯 Exigences

• Advanced degree (Masters, PhD, PharmD, MD) in health economics, outcomes research, epidemiology, biostatistics, public health, psychometrics, pharmacy, medicine, or a related quantitative or clinical discipline, or equivalent education and relevant experience • 10 or more years of progressively responsible experience in PRO, RWE, outcomes research, epidemiology, market access evidence, medical affairs, clinical research, or a related field • Substantial biopharmaceutical or healthcare-sector experience • Success defining and executing evidence strategies for complex assets, therapeutic areas, or portfolios in a global or multi-regional environment • Deep expertise in several relevant methods, including observational study design, causal inference, comparative effectiveness, economic modeling, indirect treatment comparisons, evidence synthesis, PRO/COA methods, patient preference research, or analysis of claims, electronic health records, registries, or clinical-trial data • Ability to influence senior leaders, governance bodies, and cross-functional teams without relying solely on formal authority • Experience leading complex programs, budgets, vendors, risks, competing priorities, people, and matrix teams • Strong scientific communication record and excellent written, verbal, presentation, negotiation, and stakeholder-management skills • Working knowledge of applicable research, privacy, safety, publication, compliance, and data-governance expectations • PC skills, including MS Office Suite and MS Teams • Proficiency with productivity, collaboration, presentation, project-management, and document-management platforms • Ability to travel approximately 25–30%, including domestic and international travel • Ability to participate in meetings across time zones and respond flexibly to critical business needs • Ability to perform essential functions with or without reasonable accommodation

🏖️ Avantages

• Annual bonus plan eligibility for non-commercial roles • Discretionary equity awards • Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness program

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