Medical Writer
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responsibilities:
• Supports development of clinical documents as required, including but not limited to clinical study reports, protocols and protocol amendments, and regulatory responses.
• Acts as a medical writer on single or multiple assigned projects at a simple to complex level across various therapeutic areas.
• May act as a lead writer on projects, providing internal support and/or oversight to external writers.
• Provides scientific and medical writing support and leadership to assigned product teams.
• Leads project teams in drafting document specifications, medical writing standards and requirements, and coordination and interpretation of data analysis.
• Schedules and leads peer and team review, and addresses independent quality-control review for assigned projects. You are: A well-rounded candidate who can adapt to a variety of tasks across various projects and provide good scientific leadership Here we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:
• 5 years above medical writing experience. A flexible approach to scientific writing.
• A strong scientific background, preferably with a master or above degree
• English is fluent
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