Remote Medical writing Jobs • Medical Writing

This role involves developing medical content for client engagements within the Medical Information function, which supports the safe and effective use of pharmaceutical and other products. Responsibilities include writing medical and scientific content, driving the document development process, and collaborating with teams to ensure quality and compliance. The position is home office based, requiring a valid work permit in the European Union or the UK.

The primary responsibility is to ensure all content developed is evidence-based, of the highest editorial quality, meets the strategic objectives of our clients, and translates science into clinical benefit. The SMW I is expected to effectively collaborate with all team members to drive project to efficient completion, lead content discussions with a client, and understand the strategic imperatives of the client.

Responsible for development, implementation, and maintenance of documents and/or business systems utilized for writing project support. Address and resolve issues within assigned therapeutic area(s). Interface with functional groups and writers to ensure timely completion of projects that are scientifically accurate and of high quality. Leads writing project efforts for team. Assists in selection, supervision, and project resourcing for writing team.

Primarily responsible for reviewing and confirming the accuracy of the translations for standard (and custom) response letters and FAQs in German, French, Italian, Dutch and any other relevant EMEA languages, related to Insmed products as well as communicating the information to internal and external collaborators in the respective languages, as appropriate. Supervises medical information call center activities for Europe. Responsible for EU MRC/CRC review, as appropriate. Responsible for the preparation and execution of regional medical information congress booths.