


Nate Connors, PhD, CMPP
Philadelphia, PA, USA
Medical writer, scientific director, and strategic partner with pharmaceutical, clinical, and academic clients in developing accurate and persuasive content across diverse therapeutic areas.

Skills
- Publications writing, including successful publication of over 130 journal articles on clinical trials, preclinical studies, and HEOR analyses
- Content development across diverse formats, including posters, PowerPoint decks, training programs, and website/multimedia projects
- Extensive regulatory experience, including writing regulatory content (e.g., briefing books, protocols, IBs, and INDs) and navigating medical/legal review
- Skilled communicator and strategic partner, experienced in collaborating with clients, KOLs, and cross-functional stakeholders to achieve shared objectives
- Adaptable, reliable, and able to fulfill roles ranging from providing targeted support to overseeing entire publications projects through successful completion

Therapy areas
Well-versed in most therapeutic areas, with a particular focus on oncology, immunology, and neurology.

Experience
With nearly 20 years of experience spanning rigorous scientific training, regulatory and publications agency employment, and over a decade as a freelancer, I skillfully produce complex and compelling content that adheres to regulatory standards when helping clients achieve their scientific and commercial objectives. My body of work spans the entire drug development cycle from preclinical through postmarketing across various formats including journal articles, congress presentations, multimedia, and regulatory documentation for medical affairs, promotional, and market access initiatives. I consistently deliver high-quality, strategically focused content to meet client needs amidst evolving trends in science, technology, and industry standards.

MedCommsTech – Medical Writers Collective
