Clinical Trials Disclosure Associate - Remote

Overview

The Clinical Trials Disclosure Associate will prepare clinical regulatory documents for public disclosure, ensuring compliance with regulatory requirements and maintaining document quality.

In Short

• Prepare clinical regulatory documents for public disclosure.
• Ensure consistent quality across documents.
• Collaborate with team members to resolve problems.
• Record and maintain written redaction strategies.
• Manage timelines and coordinate work across teams.
• Self-motivated and skilled in multi-tasking.
• Excellent spoken and written English skills.
• Project management skills to prioritize work.
• Basic understanding of clinical research and regulations.
• 2-5 years of experience in a biotech/pharmaceutical environment.

Requirements

• Degree with relevant experience in regulatory documents.
• Familiarity with clinical research and regulatory documents.
• Knowledge of clinical trial disclosure regulations.
• Ability to follow controlled processes.
• Strong problem-solving abilities.
• Attention to detail and follow-through skills.

Benefits

• Equal opportunity employer.
• Commitment to employee accommodations.
• Opportunity to work in a leading biotechnology company.
• Engagement in innovative human therapeutics development.