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