Hong Kong SAR
Senior medical writer and medical communications lead with 9 years’ experience across agency, pharma and biotech settings. Proven track record in building and leading writing teams, setting editorial standards, and delivering high-impact HCP and patient-facing materials with scientific rigour, clear storytelling and strong medical/legal compliance. Broad therapy-area exposure including Cardiology, Oncology, Endocrinology, Dermatology, Gastroenterology/Hepatology, Haematology, Neurology, Ophthalmology, Psychiatry, Respiratory and Rheumatology. Experienced in client strategy, KOL management, and end-to-end event content (symposia, expert meetings, advisory boards).
• Lead development of medical and marketing content for pharmaceutical clients across multiple therapy areas, ensuring scientific accuracy, readability, creativity and compliance. • Produce and quality-control a wide range of deliverables, including: symposium highlights, expert meeting reports, detailing aids, eDMs, patient booklets, slide decks, videos, dosage cards, advertisements and event collateral. • Own event content workstreams: liaise with HCPs/KOLs on presentation content, shape agendas, develop discussion questions, and provide direction for key visuals and messaging flow. • Provide tailor-made marketing and medical communications advice to clients (message hierarchy, audience segmentation, channel-appropriate tone). • Train and mentor the editorial team; support capability-building in evidence appraisal, structure, and clarity. • Line-manage junior writers, including guidance on planning, drafting, revisions and stakeholder responses.
• Managed a team of 4 medical writers: task allocation, coaching, document review, consistency and quality control. • Authored and edited promotional and medical materials for pharma clients, ensuring key messages were accurately expressed with clarity and compliance. • Supported event development and execution, including meeting materials.
• Developed marketing and medical materials for pharmaceutical clients • Assisted in event management • Performed market research on pharmaceutical products • Handled Veeva system upload
• Supported management of semaglutide clinical trials in Hong Kong. • Coordinated with investigators, nurses and pharmacists to maintain GCP/SOP compliance and data integrity. • Conducted site visits/inspections; supported AE reporting and documentation of protocol deviations. • Delivered protocol-related training and contributed to clinical trial reporting.
• Developed manufacturing and scale-up processes for haematological cancer biologic production under GMP standards (HK and Mainland China). • Supported process optimisation to improve operational efficiency and product quality.
• Supported GMP manufacturing process development (polyethylene glycol-related) for a haematological cancer biologic across HK and Mainland China.