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Global Publication Lead, Medical Affairs

67 120
Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
lead
Английский
c1
Страна
Europe/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
Global Publication Lead, Medical Affairs (Clinical Evidence and Scientific Publications): Defining and executing global publication strategies for clinical studies, including congress abstracts and peer-reviewed manuscripts, with an accent on evidence generation, publication planning, and scientific compliance. Focus on coordinating cross-functional stakeholders, managing publication timelines and vendors, and translating clinical data into strategically relevant dissemination plans.

Location: Based at the HQ in Italy or at one of hirify.global's affiliates in Europe

Salary: Minimum €67,120 annual salary for the role based in Italy; annual bonus and locally aligned compensation for other countries.

Company

hirify.global is an international research-focused biopharmaceutical group headquartered in Parma, Italy, operating in more than 30 countries with over 8,000 employees.

What you will do

  • Define global publication strategies and maintain integrated publication plans for studies included in Evidence Generation Plans.
  • Prioritize scientific data dissemination based on novelty, product lifecycle, medical and commercial needs, and geographic priorities.
  • Identify international scientific congresses and oversee abstract planning, submissions, approvals, and affiliate coordination.
  • Develop manuscript and journal strategies covering primary, secondary, exploratory, post hoc, subanalysis, and pooled-data publications.
  • Oversee manuscript writing, review, submission, revision, and publication, including relationships with medical writers and publication vendors.
  • Coordinate Global Medical Affairs, Clinical Development, Statistics, data management, Global Value & Access, and commercial stakeholders while monitoring deliverables and compliance.

Requirements

  • Advanced degree preferred: MD, PhD, PharmD, MSc in life sciences, or a related field.
  • At least 2 years of experience in a similar role within pharmaceutical companies.
  • Strong knowledge of scientific congresses, peer-reviewed journals, publication ethics, compliance standards, GPP guidelines, authorship, and disclosure requirements.
  • Excellent understanding of clinical development and evidence generation, with the ability to translate data into impactful publication plans.
  • Strong stakeholder management, cross-functional collaboration, project management, attention to detail, and timeline management skills.
  • Fluent English required for oral and written communication.

Nice to have

  • Experience in Global Medical Affairs functions.
  • Exposure to the respiratory therapeutic area.

Culture & Benefits

  • Purpose-driven environment focused on research, sustainable innovation, and ethical behaviour.
  • Inclusive workplace with a commitment to diversity and equal opportunity.
  • Pension, private medical insurance, wellbeing programme, and flexible benefits programme.
  • Annual performance bonus and compensation aligned with the local market when the role is based outside Italy.
  • Training and development resources, flexible working arrangements, remote work options, relocation support, and tax assistance for foreign colleagues.

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