Experienced Scientific Consultant Providing Technical Oversight and Project Management Solutions
Specialized background in preclinical and clinical pharmacokinetics, immunogenicity, and biomarkers
Former DABT certified study director with experience developing NAMs for toxicology risk assessments
Hands on experience at CROs developing and validating immunoassays and cell-based assays
My Approach
As a veteran of the CRO industry, I understand the importance of getting things right the first time.
I leverage my decades of experience with project management, taking the time to deep-dive into the specifics of your therapeutic project up front and developing a detailed plan for providing you with appropriate solutions that match your timelines.
After an initial meeting to exchange relevant information, we will align on strategy, deliverables, and responsibilities as well as set an expectation for the cadence and methods of your regular updates on progress and key milestones.
My job is to make yours easier.
Fill out the form below or send me an email to start our partnership journey today.
Project Management
10+ Years Managing Assay Development & Sample Testing at Preclinical & Clinical CROs
Regulatory Expertise
FDA, EMA, ICH Guidelines, 2017 DABT Certification, Nonclinical and IND-enabling Tox, GLP/GCLP, CLIA
Technical Writing
Documents for clinical and preclinical submissions, Data Transfer Specifications
