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Q&A With Christina Robinson

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Christina Robinson
PharmD, Kaiser Permanente
Location: Upper Marlboro, MD United States
Joined: Jun 12th, 2025
About   (request update)
Experience
I currently work with Kaiser Permanente as PharmD
I have 12 years of experience working in the Biotechnology and Pharmaceutical industry.
Patient Access & Clinical Operations | Kaiser Permanente
From March 2013 to Current • 13 year(s)
 Generated front-line oncology insights by managing specialty access for patients across NSCLC, HER2+ mBC, and ovarian cancer
Referral Management Assistant & Clinical Liaison | Kaiser Permanente
From March 2013 to Current • 13 year(s)
 Patient Journey Optimization: Manage the end-to-end specialty (oncology) referral pipeline, acting as the primary liaison between multidisciplinary teams to reduce time-to-treatment and identify potential candidates for clinical trial eligibility
US Medical Affairs Strategy - Oncology | AstraZeneca
From September 2024 to October 2024 • 0 year(s)
 Supported Phase III advisory board strategy by developing clinical landscape analyses and biomarker-driven literature maps in NSCLC
US Medical Affairs Strategy - Oncology | AstraZeneca
From September 2024 to October 2024 • 0 year(s)
 Strategic Evidence Generation, Regulatory Intelligence & Risk Mitigation, Scientific Narrative & Executive Communication
US Medical Affairs Extern - Oncology | AstraZeneca
From September 2024 to October 2024 • 0 year(s)
 Strategic Evidence Generation: Executed comprehensive landscape analysis and literature mapping across NSCLC and biomarker-driven pathways to inform Phase III strategic Advisory Board initiatives. Regulatory Risk Assessment: Analyzed competitor FDA warning letters and data visualizations against regulatory criteria to identify compliance gaps. Developed a risk-mitigation plan that reduced potential regulatory exposure for upcoming asset launches.
Medical Information & Field Strategy | Johnson & Johnson Innovative Medicine
From July 2024 to August 2024 • 0 year(s)
 Developed evidence-based scientific response documents and custom medical information content addressing investigational drug safety profiles
US Medical Information & Field Strategy - Neuroscience | Johnson & Johnson Innovative Medicine
From July 2024 to August 2024 • 0 year(s)
 Scientific Communications & Content Strategy, Field Medical Strategy & Alignment, Competitive Intelligence Integration
US Medical Information Extern - Neuroscience | Johnson & Johnson Innovative Medicine
From July 2024 to August 2024 • 0 year(s)
 Medical Content Creation: Authored evidence-based Standard Response Letters and custom responses to unsolicited physician inquiries regarding investigational drug administration and safety profiles. Field Medical Support: Partnered with Medical Science Liaisons (MSLs) to provide reactive clinical data summaries, equipping the field team with accurate, compliant scientific talking points.
Office of Pharmaceutical Quality - Regulatory Strategy | U.S. Food & Drug Administration (FDA)
From May 2024 to July 2024 • 0 year(s)
 Regulatory Lifecycle Oversight, Safety Signal Analysis & Process Modernization
Regulatory & Clinical Strategy Intern | RallyBio Pharmaceuticals
From May 2023 to August 2023 • 0 year(s)
 Pharmacovigilance & Strategic Communications, Cross-Functional Clinical Optimization
Clinical Development Operations Intern | Alnylam Pharmaceuticals
From May 2022 to August 2022 • 0 year(s)
 Global Clinical Data Integrity, biomarker audit across decentralized clinical sites
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