Location: REMOTE
Description:
Assists in the timely development and completion of clinical reports, summary documents, package inserts and other documents.
May oversee the electronic regulatory submission process.
Oversees and provides recommendations for the development of formats and guidelines for documentation.
Ensures effective planning and management of timelines for all aspects of technical documents.
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision.
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Job requires an understanding and application of procedures and concepts of own discipline.
The job requires attention to detail in making evaluative judgements based on the analysis of factual information.
This job typically requires a degree or equivalent and a minimum of 2 or more years experience.
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