A company is looking for a Medical Writer (Manager) to create documents related to clinical studies and regulatory interactions.
Key ResponsibilitiesIndependently authors clinical documents compliant with regulatory guidanceManages document development processes and collaborates with project teams and subject matter expertsDevelops project timelines and communicates progress, identifying potential issues proactivelyRequired QualificationsBachelor's degree in a life science discipline5 years of experience in medical writing or related field (or equivalent experience based on education level)Familiarity with global regulatory guidance (ICH, FDA, EMA)Basic understanding of the drug development process and medical conceptsProficiency in Microsoft Word and relevant software applications
Medical Writer Manager
A company is looking for a Medical Writer (Manager) to create documents related to clinical studies and regulatory interactions. ...
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Develops technical system implementation and configuration documentation and related technical support user guides and procedures guides;. Develops technical systems support and knowledgebase documents;. Reviews, validates and updates technical system and support documents. ...
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