Global Clinical Trial Disclosure Writer
Listed on 2026-10-20
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Research/Development
Regulatory Compliance Specialist
Abb Vie's Senior Associate, Trial Disclosure will provide writing support for clinical trial registrations and results postings, ensuring compliance with regulatory requirements. The role involves coordinating reviews, drafting lay summaries, and contributing to SOP development for disclosures across global sites.
Ideal candidates have 3–4 years in clinical trial registries or regulatory transparency, a health/biological sciences background, and strong communication skills.
Are you ready to take on the Global Clinical Trial Disclosure Writer role at Abb Vie Inc.?
Step into the Global Clinical Trial Disclosure Writer role at Abb Vie Inc. in Florham Park, NJ, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Florham Park, NJ, United States.
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