Holly Huntington
Director, Regulatory Affairs @ NomadX | Compliance
- Role
- Director of Regulatory Affairs at Nomadx
- Location
- Boise, ID, US
- LinkedIn followers
- 500 followers
About Holly Huntington
With over 20 years of experience driving research success across the biotech industry, I specialize in strategic and operational excellence. I am passionate about building strong partnerships—believing that relationships are the foundation of effective research and innovation.I excel at fostering a collaborative and innovative culture, streamlining processes, and ensuring quality and compliance are at the core of every project. My expertise lies in optimizing people, processes, and technology to design, implement, and execute high-impact clinical trials and non-clinical programs.As a leader, I am dedicated to developing high-performing teams through training, coaching, and mentoring, always with an eye toward succession planning and long-term growth.I love growing my personal and professional network. Feel free to connect with me or reach out directly, h••••••••@gmail.com.Skills:Regulatory Compliance (FDA, USDA, EPA.)Food Safety R&D - rapid pathogen detectionClinical Research (Phase 1-4; Product Launch)Clinical OperationsClinical Development (Protocol and regulatory submission writing/collaborating)Clinical Trials (Planning, Implementation)CRO ManagementVendor Management Clinical Monitoring (10 years\' experience)Good Clinical Practice (GCP)Therapeutic areas (Oncology, Neurology, Endocrinology, Ophthalmology, Infectious Diseases, Orthopedics, Women’s Health)Registered Nurse (RN)(Healthcare and Disease Management Experience)Clinical Trial Managment: Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Interactive Response Technology (IRT)Innovation implementationCoaching and MentoringCross Functional Collaboration
Experience
Director of Regulatory Affairs
Feb 2026 — Present · NY, US
Education
Brigham Young University
Bachelor of Science (BS), Nursing/Registered Nurse
Skills
- Regulatory Submissions
- Clinical Data Management
- Gmp
- Pharmaceutics
- Clinical Operations
- Clinical Trials
- Infectious Diseases
- CRO Management
- Clinical Research
- CRO
- Biotechnology
- Drug Development
- Good Clinical Practice (Gcp)
- Gcp
- Ich-Gcp
- Clinical Development
- Clinical Monitoring
- Edc
- Therapeutic Areas
- Ctms
- Oncology
- Protocol
- Pharmaceutical Industry
- Sop
- Fda
- Regulatory Affairs
- Data Management
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