Senior Associate, Clinical Trial Disclosure & Writing

AbbVie; North Chicago (IL); On-site; USD 80,000 - 130,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Paid time off

Job summary

AbbVie seeks a Senior Associate, Trial Disclosure to provide writing support for clinical trial registrations and results postings. You will plan and execute disclosures per regulatory requirements and assist with agency disclosures and redaction for public release.

The role involves coordinating with multiple teams to ensure timely, accurate postings. Responsibilities include writing science summaries for registries, ensuring compliance with global disclosure standards, and contributing to

Qualifications

• Bachelor's degree in a health or biological field or related area.
• 3-4 years in clinical trial registries, regulatory transparency, or drug development with a clinical background.
• Experience in medical writing and familiarity with AMWA or similar certification preferred.
• Strong project management, cross-functional collaboration, and attention to detail.

Responsibilities

• Provide writing support for clinical trial registration and results postings with timely delivery.
• Support agency disclosure, redaction/anonymization, and data access processes.
• Coordinate reviews and approvals for trial results postings across functions.
• Ensure accuracy and quality of documentation for global registries and public disclosures.

Skills

Excellent communication

Relationship management

Influencing skills

Organizational skills

Planning and execution

Team leadership

Regulatory writing understanding

Education

Bachelor's degree

Tools

Excel

Word

Job description

AbbVie seeks a Senior Associate, Trial Disclosure to provide writing support for clinical trial registrations and results postings. You will plan and execute disclosures per regulatory requirements and assist with agency disclosures and redaction for public release.

The role involves coordinating with multiple teams to ensure timely, accurate postings. Responsibilities include writing science summaries for registries, ensuring compliance with global disclosure standards, and contributing to