Stephen Huang

QUALIFICATIONS 

MBBS (Singapore) with UK GMC Licence to Practise, MRCGP (UK), 

MBA with Distinction (Sheffield), MFPM (London)

CAREER SUMMARY

Twenty-two years of industry experience as a pharmaceutical physician, holding positions of increasing seniority with several blue-chip companies, including GSK, Novartis and P&G.

Last employed position was that of medical director at Chiesi UK & Ireland for four years; direct accountability for code compliance, final medical signatory, medical information, drug safety, local clinical trials & set up MSL team; indirectly responsibility for regulatory affairs and quality control.

Currently set up as a pharmaceutical medicine consultant with 16 years as a medical signatory, experience in medical affairs strategy, product launches (global & country levels), code compliance expertise, KOL development and late phase trials. Services offered include:

Final medical signatory of medical & promotional materials
Support marketing with commercial strategy and core claims development
Support medical communications, PR and medical education, including digital platforms
KOL advocacy development and running advisory boards
Support market access with Health Technology Appraisal responses
Provide medical input to late phase clinical study designs 
Line management of medical affairs, medical information, pharmacovigilance functions
Clients included GSK Global, Sanofi, Novo Nordisk, SPMSD, Jazz, Lundbeck: acting as medical director/lead, medical signatory and product launch expert

Wide therapy area experience in primary, secondary & tertiary care: Respiratory, Cardiology, Diabetes, Oncology, Psychiatry, CNS, Vaccines & Immunology-based therapies

Ten years of clinical practice in hospitals and as a GP prior to entering the industry.

Revalidation appraiser at the Faculty of Pharmaceutical Medicine since its inception.

Twenty-two years of industry experience as a pharmaceutical physician, holding positions of increasing seniority with several blue-chip companies, including GSK, Novartis and P&G.

Last employed position was that of medical director at Chiesi UK & Ireland for four years; direct accountability for code compliance, final medical signatory, medical information, drug safety, local clinical trials & set up MSL team; indirectly responsibility for regulatory affairs and quality control.

Currently set up as a pharmaceutical medicine consultant with 16 years as a medical signatory, experience in medical affairs strategy, product launches (global & country levels), code compliance expertise, KOL development and late phase trials. 

• Held several concurrent above-country roles:
o Member of Novartis & GSK new product teams
o Member of GSK Thrombosis Centre of Excellence

Wide therapy area experience in primary, secondary & tertiary care.

Ten years of clinical practice in hospitals and as a GP prior to entering the industry.

Revalidation appraiser at the Faculty of Pharmaceutical Medicine since its inception.

MBBS, MRCGP, MBA, MFPM