Назад
Company hidden
3 дня назад

Sr Medical Writer

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Canada
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
Sr Medical Writer (Medical Communications): Developing scientifically accurate content for pharmaceutical, biotechnology, and medical device clients with an accent on clinical research, publication planning, and regulatory compliance. Focus on conducting literature reviews, interpreting data, leading client communications, and mentoring junior writers.

Location: Toronto, Ontario, Canada (Hybrid)

Company

Provides medical communications and scientific content services for pharmaceutical, biotechnology, and medical device clients.

What you will do

  • Research, write, edit, reference, and annotate scientific and medical materials, including manuscripts, abstracts, posters, congress materials, presentations, advisory board materials, newsletters, eLearning modules, and digital content.
  • Conduct literature reviews, analyze data, and prepare materials for medical, legal, and regulatory review and defense.
  • Manage content development from initiation through delivery, ensuring scientific accuracy, consistency, compliance, timeliness, and version control.
  • Serve as a scientific lead in client meetings, advisory boards, workshops, and strategic planning discussions.
  • Support publication planning by recommending authors, journals, and congresses using evidence-based rationale.
  • Mentor junior writers and collaborate with cross-functional teams on scientific accuracy and deliverable alignment.

Requirements

  • Approximately 2+ years of medical writing experience in a medical communications agency or pharmaceutical environment.
  • Advanced degree in a scientific or healthcare-related field preferred, such as MSc, PhD, PharmD, or MD; relevant bachelor's or master's degree with extensive experience may be considered.
  • Experience working with clinicians, medical experts, key opinion leaders, and cross-functional teams.
  • Strong understanding of clinical research, drug development, data interpretation, and regulatory considerations.
  • Exceptional writing, editing, analytical, communication, interpersonal, leadership, and mentoring skills.
  • Ability to work independently, manage multiple deadlines, and use Microsoft Office, Adobe Acrobat, graphing and figure-generation tools, and virtual meeting platforms.

Culture & Benefits

  • Hybrid work arrangement in Toronto, Ontario.
  • Collaboration with clients, clinicians, medical experts, and cross-functional teams.
  • Opportunities to contribute to strategic communications, publication planning, and broader organizational initiatives.

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