Medical Writer - Freelance - Officebased

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  • Proposals: 1
  • Remote
  • #33183
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GERALDINE LYNN U. has already sent a proposal.
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Experience Level: Intermediate
Additional responsibilities:

You will provide additional writing and editing services as required (e.g. for publications) as well as assisting in the production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews and other documents needed for regulatory submissions.

Assisting in quality control (review) of documents, you will Interpret and summarise data from biostatistical summary tables and listings accurately, precisely and concisely into narrative text.

In liaison with internal groups, i.e. Biostatistics, Data Management etc., you will obtain the necessary information to ensure the timely implementation of activities related to the production of reports.

With support from the Senior Medical Writer, you will interact with clients and keep the Senior Director of Medical Writing or designee informed of document status in relation to quality and timelines.

Experience and Qualification

You must possess a Life science qualification (preferably at post-graduate level) and have knowledge of clinical trial process.

A highly organised self-motivated individual, you are able to plan and organise effectively, and demonstrate expertise with grammar, syntax and format. Computer literate, you possess word processing and related PC skills.

You are a keen problem-solver with excellent written and oral communication skills. You should also have strong interpersonal skills, which enable you to win the confidence and cooperation of colleagues.

You should be fluent in English as well as the local language.

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