Job Description
Lead Analyst, R&D Technical Writing
6 month contract
Remote - EST hours
- Requirements
- Assist in the timely development and completion of clinical reports, summary documents, package inserts, and other documents.
- May oversee the electronic regulatory submission process.
- Oversee and provide recommendations for the development of formats and guidelines for documentation.
- Provide guidance and direction for completion and development of clinical and pre-clinical documents.
- Ensure effective planning and management of timelines for all aspects of technical documents.
- Work independently with minimal supervision while applying professional expertise and judgment.
- Apply principles and concepts of subject/technical discipline to resolve issues as they arise.
- Maintain attention to detail in making evaluative judgments based on the analysis of factual information.
- Qualifications
- Bachelor’s degree or equivalent required.
- Minimum of 4 or more years of applicable work experience.
- Professional mastery of a specialized field of expertise.
- Substantial applicable work experience to supplement formal knowledge.
- Ability to apply professional knowledge and technical discipline expertise in resolving issues
Apply tot his job
Apply To this Job