Medical Writer Specialist
3 days ago
As a Medical Writer at Publicis Groupe, you will be responsible for translating complex scientific and clinical information into clear and concise documents.
Job Description:We are seeking a Medical Writer with expertise in healthcare and pharmaceutical industries to join our team. The ideal candidate will have a strong understanding of regulatory guidelines and standards, as well as excellent communication skills.
The successful candidate will prepare and edit clinical study protocols, investigator brochures, and other regulatory documents for submission to health authorities. They will also contribute to the development of manuscripts, abstracts, and posters for publication in scientific journals and presentations at conferences.
In addition, the Medical Writer will communicate complex scientific and medical information to diverse audiences, including healthcare professionals, patients, and the general public. They will also prepare safety-related documents such as periodic safety update reports (PSURs), risk management plans, and other safety documents required for regulatory submissions.
The estimated salary for this position is £60,000-£80,000 per annum, depending on experience. Benefits include WFH flexibility, employee well-being programs, and equal opportunities employment.
Clinical and Regulatory Writing
- Prepare and edit clinical study protocols, investigator brochures, and other regulatory documents for submission to health authorities.
Publication Writing
- Contribute to the development of manuscripts, abstracts, and posters for publication in scientific journals and presentations at conferences.
Scientific Communication
- Communicate complex scientific and medical information to diverse audiences, including healthcare professionals, patients, and the general public.
Drug Safety Documents
- Prepare safety-related documents such as periodic safety update reports (PSURs), risk management plans, and other safety documents required for regulatory submissions.
Regulatory Submissions
- Collaborate with cross-functional teams to compile and write sections of regulatory submissions, such as New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), and Investigational New Drug (IND) applications.
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