Director, Patient-Centered Outcomes

🕒 il y a 11 jours

🌐 États-Unis, Royaume-Uni – Distant

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

🍂 Massachusetts – Distant

🍂 Massachusetts – Remote

⏰ Temps Plein

🟠 Senior

👔 Directeur

👻 Score fantôme 10%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.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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Lumanity

Site WebLinkedInTous les Emplois

1001 - 5000 employés

Fondée en 2020

🏥 Santé

💼 Conseil

📦 Logistique

Healthcare • Consulting • Logistics

Lumanity se concentre sur l'amélioration de l'expérience des candidats grâce à des solutions numériques modernes. Les initiatives de l'entreprise incluent la rationalisation du processus de candidature et l'utilisation de données anonymes pour améliorer l'interaction des utilisateurs sur leur plateforme. Ils mettent l'accent sur la confidentialité et la conformité dans leurs opérations, garantissant que les données des candidats sont traitées avec soin et transparence.

Description

• Provides strategic and scientific leadership for patient-centered outcomes engagements • Ensures research design, execution, and evidence packages are fit-for-purpose for client decision-making and regulatory use • Leads clinical outcome assessment projects, including literature reviews, gap analyses, COA development and modification, in-trial interviews, regulatory strategy, and dossier development • Defines scientific approaches by translating client objectives into tailored research designs and evidence-generation plans • Develops endpoint and regulatory strategies for COA evidence packages supporting labeling claims • Leads project teams by defining methodological approaches, confirming data requirements, and ensuring deliverables address research questions • Reviews analyses, data interpretations, and client deliverables for scientific integrity, accuracy, scope alignment, and intended use • Guides client interactions, frames options, communicates recommendations, and aligns stakeholders on research and evidence-generation decisions • Ensures timely, high-quality delivery across the project portfolio, monitors execution, and course-corrects as needed to achieve annual revenue targets • Expands existing accounts and develops new client opportunities • Leads proposal development, including scoping and budgeting, and delivers against annual sales targets • Provides direction and role-relevant technical training to junior project team members

🎯 Exigences

• Master’s or doctorate degree in a health-related field preferred, not required • Minimum 8 years of progressive experience leading PCO and COA research, with accountability for scientific and strategic direction of endpoint evidence generation to support medical product labeling claims • Demonstrated expertise in developing COA strategies informed by literature reviews and gap analyses, delivering strategic insights aligned to the client’s clinical, regulatory, and reimbursement objectives • Demonstrated expertise in qualitative research and COA-focused methodologies, including standalone COA development/modification studies and the design, implementation, and execution of clinical trial interviews • Demonstrated ability to develop endpoint and regulatory strategy for assigned projects by applying regulatory guidance and precedent to evidence plans, regulatory interaction support, and regulatory documentation • Demonstrated expertise in methodologies required to deliver additional PCO service offerings, including Delphi panels and survey research, patient preference studies, discrete choice experiments, and goal attainment scaling; desired but not required • In-depth understanding of the drug development process, including experience navigating COA development with regulators and developing evidence to support medical product labeling claims • Proven ability to lead multidisciplinary project teams delivering multiple concurrent engagements while maintaining scientific quality, timeline adherence, and clear decision-making • Strong analytical and writing capability, including synthesizing complex evidence into clear, defensible client recommendations and fit-for-purpose deliverables • Strong client-facing communication skills, including the ability to lead senior stakeholder discussions, present recommendations, and address complex scientific and strategic questions with clear, well-supported responses • Demonstrated business development capability, including leading proposal scoping and budgeting, and contributing to sales and revenue generation

🏖️ Avantages

• Competitive salary plus bonus scheme • Medical, dental, and vision insurance options • 401(k) plan with employer match • Flexible paid time off program + 10 paid holidays • Flexible spending accounts for health and dependent care • Health savings account option with employer contribution • Employee Assistance Program • Paid short-term and long-term disability coverage • Company-paid life insurance coverage at 1.5x annual salary • Paid parental leave and more