Leen E.
Medical Information Specialist @阿斯利康
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WORK HISTORY
Medical Information Specialist @阿斯利康
Medical Information Specialist supporting AstraZeneca’s portfolio across Respiratory, Immunology, Vaccines, and Immunotherapy, delivering high-quality, compliant, and timely scientific information to healthcare professionals. • Manage and respond to complex medical information enquiries, providing accurate, evidence-based, and balanced responses in line with regulatory and compliance requirements. • Support oncology patients and their HCPs through the management of Named Patient Supply (NPS) and bridging therapy schemes, ensuring continuity of care and close coordination with internal and external stakeholders. • Lead vendor management activities, including onboarding, training, quality oversight, and performance monitoring to ensure consistent delivery of medical information services. • Own and manage the HCP Medical Information Website for reactive use, continuously maintaining, optimising, and improving content, usability, and scientific accuracy. • Work cross-functionally with sales representatives and field force teams to effectively signpost healthcare professionals to approved digital medical information resources, supporting appropriate access to scientific content. • Contribute to the continuous improvement of medical information processes, digital engagement, and customer experience across therapy areas.
EDUCATION
Kingston University
Bachelor's degree, Pharmacology
Queen Mary University of London
Master of Science - MSc, Clinical Drug Development
ABOUT LEEN E.
As a BSc (Hons) Pharmacology graduate from Kingston University and current MSc Clinical Drug Development student at Queen Mary University of London, I bring a strong foundation in medical science and a forward-thinking approach to pharmaceutical industry challenges.In my current role at Britannia Pharmaceuticals Ltd, I lead medical information activities across multiple advanced Parkinson’s Disease therapies. I am the primary contact for escalated inquiries, oversee the development of Standard Response Letters (SRLs) and SOPs, and spearhead an internal project to automate enquiry workflows and enhance reconciliation processes. I also manage internal and external product training.My responsibilities extend into global medical affairs, where I lead high-impact initiatives such as Delphi Panels, international Advisory Boards, and nurse faculty meetings. I ensure strategic and compliant execution of events, medical writing, and cross-functional stakeholder engagement—all aligned with ABPI Code standards.With hands-on experience in Veeva Vault, compliance workflows, content development, and customer engagement operations, I bridge scientific communication with commercial strategy. I’m passionate about improving patient outcomes through accurate, accessible, and compliant medical information; and I thrive in dynamic, collaborative environments where innovation and detail matter.
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