Senior Medical Writer - UK/EU
5 days left
- Experience Level
6-12 month contract
Home based in UK/EU - open to candidates from any European country
Competitive hourly rate
Provides high-quality medical (Regulatory) and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients.
Independently researches, writes, and edits clinical study reports, study protocols and standard response documents.
Produces complex clinical or scientific documents, such as, IBs, and sections of INDs, NDAs, CTDs, and dossi
Education and Experience:
- Must have breadth of regulatory writing experience (including, but not limited to clinical protocols, informed consents (ICFs), clinical study reports (CSRs), investigator brochures (IBs), patient narratives, annual reports, and other key clinical and regulatory submission documents).
- Bachelor's degree in a scientific, medical or clinical discipline or related field required, PhD preferred
- Minimum of 5 years of pharmaceutical/biotechnology Regulatory Writing experience required
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