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4 дня назад

Senior Consultant, Evidence Generation (Real-World Evidence)

55 800 - 83 800€
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Italy
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Consultant, Evidence Generation (Real-World Evidence): Developing end-to-end real-world evidence strategies, study designs, proposals, and client solutions for Medical Affairs, Market Access, and HTA stakeholders with an accent on observational research, implementation science, hybrid studies, and synthetic data applications. Focus on leading complex consulting engagements, assessing data and study feasibility, coordinating cross-functional project teams, and shaping new evidence-generation opportunities.

Location: Milan, Italy

Salary: €55,800–€83,800 annualized base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Act as a senior RWE consultant and strategic partner to Medical Affairs, Market Access, and HEOR stakeholders.
  • Translate evidence needs into tailored evidence-generation strategies aligned with regulatory and HTA requirements.
  • Lead or contribute to RWE proposals, client-ready solution materials, study designs, and commercially sound delivery models.
  • Design innovative approaches including implementation science studies, hybrid studies, and synthetic data applications.
  • Scout and support activation of new data sources, clinical networks, and partnerships.
  • Coordinate cross-functional project teams, manage client communication, review deliverables, and develop follow-on business opportunities.

Requirements

  • Master’s degree in Life Sciences, Pharmacy, Medicine, Data Science, Biomedical Engineering, or a related field.
  • 5–8 years of senior experience in Real-World Evidence, Observational Research, Evidence Generation, or HEOR within a CRO, life-sciences consultancy, pharmaceutical organization, or biotechnology organization.
  • Strong knowledge of RWE and non-interventional research across the product lifecycle.
  • Ability to align evidence plans with Medical Affairs, Market Access, regulatory, and HTA requirements.
  • Experience in client-facing consulting, proposal leadership, business development, feasibility assessment, and bid-defense support.
  • Strong analytical and strategic capabilities for assessing data availability, study feasibility, operational implications, evidence-generation approaches, new data partners, and innovative evidence models.
  • Strong project leadership, communication, and stakeholder-management skills.
  • Ability to work effectively in a cross-functional and international matrix environment.
  • Proven sell-deliver leadership in complex RWE environments, including evidence strategy design and project management across multiple stakeholders, therapeutic areas, and methodological approaches.

Nice to have

  • PhD in a relevant field.

Culture & Benefits

  • Full-time employment in an international, cross-functional environment.
  • Base pay varies according to qualifications, skills, education, experience, location, and schedule.
  • Potential incentive plans, bonuses, health and welfare benefits, and other benefits may be offered depending on the position.
  • Integrity and truthful, complete application information are required.

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