Great Location
Competitive Salary
Performance Bonuses

Medical Writer/Senior Medical Writer

Vacancy Salary £Competitive
Vacancy Location Cambridge
Mergefield Title {Mergefield Value}
Mergefield Title {Mergefield Value}

This is a Permanent, Full Time vacancy that will close in {x} days (x will be populated when viewing published adverts).

Kymab is a clinical-stage biopharmaceutical company developing a deep pipeline of novel antibody-based therapies in a broad range of indications. The Company generates its product candidates using its proprietary, integrated platforms collectively called IntelliSelect®. Kymab’s platforms have been designed to maximize the diversity of human antibodies produced in response to immunization with antigens. Selecting from a broad diversity of fully human antibodies allows for the identification of antibodies with optimal drug-like properties.



  • To prepare, edit and review medical, regulatory and clinical documents to support Kymab development programmes including clinical study protocols, investigator brochures, non-clinical summaries, briefing documents, safety/efficacy summaries and clinical study reports, as well as scientific publications and communications to journals and conferences.
  • To drive and coordinate the development of cross-functional documents to ensure completion to timelines.
  • To work closely with subject matter experts ensure their writing is of the highest standard of technical accuracy.
  • To support clinical and regulatory teams to ensure that amendments to documents are clearly and accurately captured.
  • To develop and support QC processes to ensure quality and accuracy within and between development documents.
  • To assist in the development of templates for core documents that ensure the compliance and consistency
  • To work with key functions to develop Kymab’s house style to create a consistent and high quality image across Kymab documents.




Education and Experience

  • Degree level education or higher
  • At least 5 years’ experience of medical writing within the pharmaceutical industry or contract research organisations
  • Experience in writing for clinical trials across a range of therapeutic areas and geographies, preferably with substantial Oncology experience


Skills and Knowledge

  • Excellent written communication skills
  • Ability to adapt writing style to a range of different audiences
  • Advanced competency with writing tools including Word, powerpoint, prism, and reference management tools e.g Zotero, Mendeley etc.
  • Knowledge of GCP and related regulatory guidelines governing clinical trials in the UK, EU & USA


  • Excellent attention to detail
  • Highly organised, able to prioritise work, work well under pressure and meet deadlines
  • Team player able to work in a flexible, collaborative style with colleagues and teams within the company and with external advisors including CROs and consultants.
  • Ability to see complex projects to completion


Kymab embraces diversity and equality of opportunity and are committed to building inclusive and diverse teams representing all backgrounds. We welcome and consider applications to join from all qualified candidates, regardless of their characteristics.

We are a young, passionate and determined company.

We want to succeed in our aims to make a difference in healthcare and make better medicines using our unique technologies.

Our headquarters are in Cambridge, UK, on the Babraham Research Campus, an established bioscience campus, home to more than 60 companies.

Since we were founded, our team has grown to more than 180 people. It’s an invigorating environment where our teams work closely and collaboratively to help us all to achieve our aims.

You’ll find your role at Kymab exciting, interesting and stimulating, with the opportunity to interact with a diverse range of colleagues, both internally and externally.

Great Location

Competitive Salaries

Performance Bonuses

Share Plan

Healthcare Cover

Life & Income Insurance

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