Court of Patrons




Deputy Director/Chief Operating Officer

TRI Medical Writer

Will be responsible for creating high-quality written materials across a range of media, including slides, manuscripts, posters, meeting reports and websites in collaboration with our clinical advisors and PR team.

Job Description:

The Medical Writer will contribute to the development of high-quality, medically accurate documents, in the field of thrombosis, addressing different target audiences. Depending on the scope and nature of each project, this responsibility will include: content development (writing), editing, conducting background research, data checking, reference annotation and taking minutes at meetings. Other responsibilities will include assistance with strategic publication planning and meetings’ support.

Key Responsibilities:

  • Content development of written materials (e.g. abstracts, posters, slides, manuscripts, and a wide range of other medical communication activities)
  • Builds an increasing knowledge of the science/medicine of thrombosis to the degree required for effective communication with internal team members, clients, authors and target audiences
  • Conducts searches of the published medical literature and other sources of medical, marketing and drug development information as directed by TRI team members
  • Maintains and organizes electronic reference libraries using EndNote
  • Uploads files and complete submission for abstracts and manuscripts
  • Maintains the publication plans for various TRI studies
  • Works with multidisciplinary project teams and external advisors to ensure projects are delivered within-budget, on-time and on-message
  • Occasional travel, including international travel, required


  • A sound scientific understanding and strong writing ability
  • An aptitude for interpreting data and distilling complex scientific information into engaging and effective content, with a keen attention to detail and accuracy
  • Ability to find and correct errors in spelling, punctuation, grammar and check text for consistency, clarity and accuracy
  • Excellent communication and interpersonal skills
  • A high level of personal motivation and initiative
  • The ability to work independently and effectively in a team across multiple projects
  • A flexible and proactive attitude, with the ability to prioritize and work to tight deadlines without compromising quality

Desirable Qualifications/Experience

  • A PhD or MSc in life sciences
  • At least 1 years previous experience as a Medical Writer in the life sciences
  • Some project management experience
  • A basic understanding of statistics
  • Experience in working with collaborative, cross-functional teams
  • Knowledge of the pharmaceutical industry and processes

All interested candidates are required to complete a writing test.

Candidates must be eligible to work in the UK in order to be considered for this role.