Remote: Yes

Willing to relocate: No, but willing to discuss a mutually agreed schedule of traveling to the office (e.g. once a quarter)

Key experience as regulatory lead: IND, CTA, and sNDA filings, responses to FDA and global health authority queries, orphan drug applications, substantial amendments

Résumé/CV: please email for CV

Email: dyhndz [at] gmail [dot] com

Hi, I am a highly motivated and business-minded regulatory affairs professional with diverse experience seeking employment at a biotechnology or pharmaceutical company. I am open to clinical regulatory strategy roles at a variety of company types and therapeutic area focus, including traditional pharma and AI-based biotech startups alike, just to name two differing examples.

My experience is spread across the biotech startup space, top 10 big pharma, government laboratory, and a contract research organization. Most recently, I functioned as regulatory strategy lead at the mid-senior level for a small molecule anti-seizure medication. I would be happy to discuss how my abilities as a regulatory strategy lead and varied experience in the biopharma field could contribute to advancement of your product pipeline, mesh with your current teams and style of regulatory affairs, and add value to your company.