Teams at Johnson & Johnson

Manage production of plain language summaries (PLSs) for clinical trials, ensuring scientific integrity, regulatory compliance, vendor oversight, cross-functional alignment, and timely delivery while applying health-literacy principles and protecting confidential participant and IP information.

Lead production of plain language summaries (PLS) for clinical trials, ensuring scientific integrity, regulatory compliance, and readability for lay audiences. Oversee vendors, review drafts, align with clinical teams and stakeholders, apply regional PLS requirements (e.g., EU CTR), manage templates/SOPs, facilitate translation hand-offs, and track metrics and risks to improve scalable PLS processes.

The Senior Scientist Clinical Pharmacokinetics will oversee clinical trial protocol development, pharmacokinetic analysis, data reporting, and mentorship of junior scientists, ensuring compliance with regulatory standards.