AbbVie

Lead and mentor a dedicated team of talented safety physicians (medical, senior medical, and group medical directors) responsible for safety oversight of all assets in the Oncology Early Development (OED) portfolio.

Responsible for driving the safety strategy for products in OED by understanding the complexities of the treatment landscapes and enterprise-wide strategic goals, working closely with stakeholders across all functions and stages of drug development, and above all understanding the needs and goals of patients, care-givers, and physicians fighting devastating diseases in oncology.

Executive Medical Director for Oncology Early Development Safety

Manage a group of Product Safety Team Leads (physicians) supporting primarily IO programs in Oncology Early Development.

Group Medical Director

Genentech

Senior Medical Safety Director

Safety science lead for oncology and immuno-oncology products in early clinical development. Responsibilities include: anticipating and characterizing the safety profile of new drugs from pre-IND/CTA through early clinical development, oversight for medical review of individual case safety reports and reporting to health authorities, writing and oversight of regulatory safety-related documents, and working on cross-functional teams to help ensure safety risks are managed in a way that creates value to patients through effective and timely therapies for devastating diseases.

Medical Safety Director

Senior scientist in the department of clinical pharmacology serving as the clinical pharmacology lead on development programs in the oncology and immuno-oncology pipeline. Additional roles included serving as Pharmacology Sub-Team Lead (PSTL) with oversight for preclinical and nonclinical development strategy.

Senior Scientist - Clinical Pharmacology

Walter Reed Army Institute of Research

Manage an internationally renowned clinical trial center conducting phase 1 and 2 clinical trials of vaccines and drugs combating several infectious diseases including malaria and many viral diseases such as Ebola, Dengue, MERS-CoV, and Zika. Responsibilities include functioning as principal and associate investigator, building and fostering relationships with outside entities, clinical trial design and protocol writing, manage a budget of several million dollars annually, regulatory and IRB submissions, and personnel management.

Director, Clinical Trial Center

Serve as principal and/or associate investigator on over 20 clinical studies for infectious disease products (vaccine and small molecule) in phase 1 and 2. Serve as medical monitor and safety physician for clinical studies outsourced to CROs.

Clinical Investigator/Medical Monitor

Program Director - Clinical Pharmacology Fellowship

Chief of Clinical Pharmacology

Fort Belvoir Army Community Hospital

Internal Medicine Physician

Multinational Force and Observers

Officer in Charge of a clinic of 6 military physicians from US, Uruguay, Fiji, Colombia, and Hungary, and 20 medics from the US army. Physician serving as primary care manager for nearly 1,200 soldiers/civilians stationed at or living at the MFO. Coordinated MEDEVAC. Worked with partner facilities in Israel for tertiary care needs. Served as medical adviser to battalion commander, US brigade commander, and the Force Commander (a NZ Maj. Gen.) Also functioned as acting company commander for roughly 60 soldiers in a medical company in commander's absence.

Officer in Charge - Clinic and Clinic Staff

Physician/Scientist with expertise in clinical pharmacology, early stage clinical trial design and execution, drug safety, pharmacovigilance, and regulatory science for small molecules, protein therapeutics (monoclonal antibodies, T cell bispecific antibodies, immune checkpoint inhibitors), gene and cell therapy, and vaccines in oncology, immunology, and infectious disease. I am board certified in clinical pharmacology and internal medicine with more than 14 years of clinical experience and 10 years of experience in the pharmaceutical and biotechnology sectors, primarily serving on cross-functional development teams as a safety physician, medical monitor, principal investigator, and/or clinical pharmacologist on a variety of products. 

In addition to my medical and regulatory expertise, I have my MBA from Kenan-Flagler Business School at UNC and I am a veteran of the US Army where I had several years of experience leading teams of 20-40 people.

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