Princeton, New Jersey, United States
- Over 13 years of experience in both Medical Affairs/Scientific Communications and clinical practice across diverse therapeutic areas, including Nephrology, Immunology, Psychiatry, Rare Disease, Rheumatology, Cardiovascular Disease, and Hematology. - Demonstrated track record of shaping global communication strategies, leading development of high-quality, evidence-based scientific content, and driving cross-functional alignment essential for pre-launch, launch, and post-launch activities for numerous pipeline and marketed assets. - I bring an innovative, collaborative, detail-oriented mindset to every project, with a commitment to improving processes, enabling teams, and ensuring scientific rigor across all deliverables. - Ability to establish and maintain relationships with internal and external stakeholders. - Proven ability to translate complex clinical data into accessible, meaningful materials that support scientific exchange throughout a products life cycle. - Highly developed communication skills, including presentations to large groups, interactive discussions, and 1:1 discussions with key thought leaders.
As Associate Director of Global Medical Information, I led the strategic development and execution of global scientific content and communication initiatives that ensured the delivery of accurate, compliant, and impactful medical information across multiple therapeutic areas. Key Contributions & Responsibilities: -Leading global medical communication content strategy and lifecycle management for pipeline and marketed products, including LUPKYNIS®, JYNARQUE®, ABILIFY MAINTENA®, REXULTI®, and Sibeprenlimab. -Driving launch readiness and scientific content development to support pre-launch, launch, and post-launch phases across global markets. -Partnered cross-functionally with Medical Strategy, Scientific Communications, and Field Medical Affairs to ensure unified, evidence-based messaging aligned with brand and corporate objectives. -Oversaw the creation and maintenance of Standard Response Documents (SRDs), FAQs, Data-on-File, and Medicaid testimonies, ensuring compliance with medical and regulatory standards. - Developed and executed medical training programs, reference resources, and content management systems to ensure consistent, compliant, and high-quality scientific communications. -Spearheaded the Interactive standard response letter framework, pioneering how medical content is accessed, visualized, and utilized across cross-functional teams. -Generated and interpreted Medical Information insights and analytics, transforming data into strategic recommendations that inform Medical Affairs planning. -Mentored and developed global MI professionals, fostering a culture of excellence, collaboration, and continuous improvement across regional teams. Core Impact: Strengthened the global consistency and quality of scientific communications. Improved operational efficiency through innovative knowledge frameworks. Supported multiple successful product launches across key therapeutic areas.
• Prepared and compounded sterile IV preparations in compliance with FDA and USP <797> requirements. Preparations included pain management (anesthetics, opiate agonists) and chemotherapy admixtures, antibiotics, TPNs, anti-coagulation therapy, neuromuscular blocking agents, and oxytocics. • Supervised IV pharmacy technicians and ensured adherence to aseptic techniques and cGMP regulations.
• Provided evidence-based responses to healthcare professional inquiries using scientific literature and internal resources. • Created educational resources for patients and HCPs to support medication safety and adherence. • Conducted medication reviews and dosing evaluations to ensure optimal clinical outcomes.
• Provided frequent medication counseling and drug utilization reviews (DURs) for patients that were chronically ill, elderly, immunosuppressed, or suffering from mental illness. • Knowledge of formulary alternative management, medication compliance issues, and adverse drug event/drug interaction reporting and management.
•Developed and screened patient profiles for possible medication discrepancies, duplications of therapies, interactions, gaps •Performed DUR's and identified drug related problems/ interactions •Controlled substance inventory •Verified and dispensed proper medications in a safe and efficient manner •Monitored technician duties and aseptic compounding techniques •Administered routine vaccinations