Senior Associate, Trial Disclosure - Remote

Overview

The Senior Associate, Trial Disclosure will provide writing support to clinical trial registration and results postings, ensuring compliance with regulatory requirements while managing multiple projects.

In Short

• Responsible for writing and disclosing clinical trial information globally.
• Provides medical writing expertise across multiple therapeutic areas.
• Implements changes in regulatory requirements and develops SOPs.
• Coordinates review and approval processes for clinical trial results.
• Manages timelines and quality for writing projects.
• Identifies and resolves conflicts in project deliverables.
• Supports anonymization and redaction of clinical documents.
• Writes summaries for complex study designs per global registry requirements.
• Communicates effectively across functional areas.
• Maintains attention to detail while prioritizing tasks.

Requirements

• Bachelor's degree in health or biological science required.
• 3-4 years of experience in clinical trial registries or drug development.
• Preferred experience in medical writing in healthcare or academia.
• Knowledge of project management practices.
• Excellent communication and organizational skills.
• Ability to work in an international environment.
• Working knowledge of registration and agency disclosure requirements.
• Proficient in Excel, Word, and other relevant systems.
• Strong ability to interpret scientific content.
• Superior attention to detail and ability to meet deadlines.

Benefits

• Comprehensive benefits package including paid time off.
• Medical, dental, and vision insurance.
• 401(k) plan for eligible employees.
• Participation in short-term incentive programs.