Lead Analyst, R&D Technical Writer
Job in
Duluth, St. Louis County, Minnesota, 55806, USA
Listed on 2026-06-03
Listing for:
GForce Life Sciences
Full Time
position Listed on 2026-06-03
Job specializations:
-
Research/Development
Job Description & How to Apply Below
- 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.
- 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
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