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A leading global clinical research organisation is seeking a Medical Writer II to support clinical submissions and author complex documents. The role involves significant responsibilities including project management and stakeholder coordination, offering a chance to contribute to vital therapies reaching the market. Ideal candidates will have medical writing experience and previous project lead roles, especially in Phase I - III studies.
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Planet Pharma is currently working with a global clinical research organisation (CRO) that is looking for an experienced Medical Writer to join their team and support the preparation of submission and other complex clinical documents.
As part of this role, you will be responsible for authoring most study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. You will also be responsible for:
This is an exciting opportunity to join a globally renowned CRO and play a significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor and will have the chance to take on project management responsibilities.
For this position, the client is seeking someone with experience as a medical writer and prior experience working as a project lead on medical writing projects.
You should also have experience with:
For more information on this position or similar opportunities, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to chanel.hicken@planet-pharma.co.uk. We can then arrange a confidential discussion on how you can get involved in this exciting opportunity.