Scientific Publications Lead

Pharvaris
•$140,000 - $185,000•Hybrid

About The Position

Pharvaris is a Nasdaq-listed late-stage biotech company developing bradykinin B2 receptor antagonists for bradykinin-mediated diseases. We aim to bring new, more convenient options to HAE patients who suffer sudden and prolonged attacks of swelling in multiple areas of the body, including the airway, which can be life-threatening. Our company culture is built on core values of considering others carefully, leading with trust, ensuring rigor and diversity of thought, and contributing freely. We are driven by individuals committed to developing breakthrough therapies that can have a real impact on people’s lives. As we expand the global Medical Affairs team, we are looking for a Scientific Publications Lead to join our team and report to the Executive Director, Head of Medical Communication.

Requirements

  • Advanced scientific degree (PhD, PharmD, MD or MSc), preferably in life sciences or another health-related field.
  • Preferably 5 years+ global experience in publication management or medical communications (in a pharmaceutical/biotech environment), ideally in the field of rare disease or more specifically hereditary angioedema (HAE).
  • Preference for candidates who have worked for emerging biopharmaceutical companies in the past, with evolving operating procedures and employee remits.
  • Prior leadership or cross-functional team experience (managing vendors, overseeing projects, leading publications planning).
  • Experience in working in a highly regulated environment, preferably familiar with ICMJE, GPP, and other international standards for ensuring the quality and transparency of publications.
  • Proficiency using medical/scientific publication databases/resources and project software.
  • Proficiency in Microsoft Office (Word, PowerPoint, Excel, Outlook).
  • Good attention to detail with critical and analytical skills.
  • Excellent communications skills (verbal and in writing).
  • Excellent project management skills.
  • Problem-solving skills and result-oriented.
  • Strong team player and an international mindset.
  • Natural ability to influence and lead projects.

Responsibilities

  • Partner with the wider cross-functional and MedComms team to support the global scientific publications strategy.
  • Execution of the global scientific publication’s strategy, ensuring alignment with the medical and company strategy.
  • Developing, managing, and delivery of the annual publications plan, including manuscripts, abstracts, congress presentations, and posters.
  • Manage the end-to-end publications process from development to journal submission and congress presentation.
  • Manage relationships with KOLs, authors, and external vendors to facilitate smooth collaboration and timely publication.
  • Lead and manage the exploration and development of novel publication analysis to drive and sustain long-term communication of deucrictibant's value proposition.
  • Oversee the creation of high-quality scientific content, ensuring all publications adhere to Good Publication Practices (GPP) and industry standards.
  • Development of enduring scientific communication materials.
  • Translate complex scientific data into clear, compelling, and compliant medical content for diverse audiences, including medical education materials.
  • Partnering cross-functionally with Medical Affairs, Patient Advocacy, Early Development, Clinical Development, and Evidence, Value, and Outcomes Research to develop and align publication strategies aligned with company imperatives.
  • Supporting advisory boards, speaker programs, medical education activities, and (scientific) symposia with key publications and medical content.
  • Maintain awareness of the latest trends and advancements in the pharmaceutical industry to drive innovation and improve publication practices.
  • Work closely with the legal and compliance team to ensure all ethical information and publications activities meet legal and ethical standards.
  • Ensure proper archiving and documentation of publication materials in compliance with company policies and regulatory requirements.
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