Senior Medical Writer

Yseop specializes in artificial intelligence (AI) and is a recognized pioneer in Natural Language Generation (NLG) technology. Yseop is rapidly expanding globally, providing enterprise-level automation solutions for some of the world's largest companies in a variety of industries including finance , pharmaceuticals and computer software company .

With its multi award-winning Language AI technology, Yseop is revolutionizing the way analysis and reporting is done. Yseop's powerful and user-friendly t platform allows business users to seamlessly and quickly build and automate the generation of text reports from any structured data.

At Yseop, our mission is to support companies through this digital transformation. We believe that our cutting-edge artificial intelligence technology allows businesses to increase the efficiency of their operations and shift employee time spent on tedious tasks to more value-added and creative work.

So join Yseop and be part of an amazing adventure that is only at its beginning

Our corporate values drive our daily job:

• Team : We care about each other, inspire each other and encourage strong team spirit
• Trust: Trust is foundational. It empowers our employees and customer relationships.
• Innovation: We love to innovate in ways that delight our customers
• Customer Centric: We exceed customer expectations and aspire to create true partnerships.
• Fast: We practice agility, prioritize simplicity and we are proactive

We are building a diverse and inclusive team - and we need your help

So join us to build tomorrow, today,

Your mission

Are you passionate about creating high-quality, impactful medical writing while working with cutting-edge technology?

Join Yseop as a
Medical Writer with Safety Writing experiebce
, where you'll play a key role in configuring and validating our AI-driven solutions.

Your responsabilities will be :

• Define content requirements and templates for automating the generation of pharmacovigilance
  regulatory documents.
• Collaborate with the product team to
  translate regulatory requirements into structured, configurable content models
  that support automation.
• Ensure that generated documents meet
  ICH, EMA, FDA, and other global regulatory standards
  for PV reporting.
• Provide expert
  guidance on data-driven document generation
  , structuring narratives based on PV safety databases and case reports.
• Review and validate
  AI-generated content for compliance, accuracy, and consistency.
• Work closely with UX/UI teams to ensure the medical writing workflow is intuitive and efficient for end users (pharmacovigilance professionals and medical writers).
• Monitor regulatory updates and industry trends to adapt and improve automation models.

Required Qualifications & Experience

• Extensive experience
  (5+ years) in medical writing focused on pharmacovigilance regulatory documents.
• Deep understanding of
  Clinical documents & global PV regulations
  (ICH E2E, E2C, E2F, GVP modules, FDA, EMA, and MHRA guidelines).
• Experience working with
  PV safety databases
  (e.g., Argus, ArisG, Veeva Vault Safety) and structured data for case reporting.
• Knowledge of
  document automation, structured authoring, or AI-generated content
  is a plus.
• Ability to collaborate cross-functionally with
  product managers, engineers, and regulatory teams
  .
• Strong attention to detail and the ability to define
  clear, standardized templates and content rules
  .

Preferred Skills

• Familiarity with
  authoring tools and automation platforms
  for regulatory writing.
• Experience in
  technology-driven projects
  , such as integrating medical writing with AI/NLP tools.
• Strong problem-solving skills and an interest in
  streamlining and improving regulatory document workflows
  .

Your profile

• Expertise in medical writing, Clinical Documents & PV documents
• Familiarity with AI-driven or data-to-text technologies is a plus.
• Strong editing and quality assurance skills.
• Excellent communication and collaboration abilities.
• Ability to manage multiple projects and meet strict deadlines.

Yseop is an equal opportunity employer. We believe diversity is a strength and fosters innovation. We are committed to enabling everyone to feel included and valued at the workplace. All qualified applicants will receive consideration for employment without regard to age, color, family, gender identity, marital status, national origin, physical or mental disability, sex (including pregnancy), sexual orientation, social origin, or any other characteristic protected by applicable laws.