Trial Disclosure Writer – Regulatory Registrations

AbbVie Inc.; North Chicago (IL); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid time off

Health insurance

Dental insurance

Vision insurance

401(k)

Job summary

AbbVie Inc. is seeking a Senior Associate, Trial Disclosure to support clinical trial registrations and results postings. You will write scientific results and lay summaries, ensuring timely and accurate public disclosures according to regulatory requirements.

The role involves planning registration activities, SOP implementation, and collaboration across departments to meet deadlines with high-quality output. Experience in medical writing and regulatory transparency is essential.

Qualifications

• Bachelor's degree in health or biological science required.
• 3-4 years experience in clinical trial registries, regulatory transparency or drug development.
• AMWA certification preferred; with editing/writing specialty.
• Strong project management and cross-functional teamwork skills.
• Excellent written and verbal communication.

Responsibilities

• Complete writing activities to ensure timely disclosure of accurate information globally.
• Provide medical writing expertise for multiple compounds/projects.
• Implement SOPs/process improvements and training activities.
• Communicate deliverables and timelines across teams.
• Coordinate review and approval for trial results postings and agency disclosure.

Skills

Bachelor's degree

3-4 years experience

AMWA certification

Editing/Writing

Project management

Cross-functional teamwork

Excellent communication

Education

Bachelor's degree in health or biological science

Tools

Excel

Word

Job description

AbbVie Inc. is seeking a Senior Associate, Trial Disclosure to support clinical trial registrations and results postings. You will write scientific results and lay summaries, ensuring timely and accurate public disclosures according to regulatory requirements.

The role involves planning registration activities, SOP implementation, and collaboration across departments to meet deadlines with high-quality output. Experience in medical writing and regulatory transparency is essential.