Shiow Wei Goh

Experienced leader in Life Sciences advisory, working with a range of Pharma & Biotech companies (global scale, mid-cap, PE backed) on driving strategic decisions through to operational performance. Key features of my advisory and delivery experience:

• Enterprise value engineering - working with senior stakeholders to identify value opportunities to drive business growth and innovation, optimise margin and cost. This involve bringing a holistic understanding of the R&D value chain across clinical research, clinical development, regulatory affairs, drug safety / pharmacovigilance, medical affairs, and quality.
• Operating model transformation - designing and implementing operating models to enhance capability leadership of the business, optimise global/local/outsourcing models, optimise footprint and organisational design. Often this is resulting from M&A activities, growth in markets / business consolidation, enterprise cost reduction.
• Digital transformation and Process optimisation - helping life science organisation to adopt new technology e.g. AI at an enterprise level (from ideation, through to adoption and scaling). This also include process transformation to reimagine how work is delivered, leveraging techology and process mining capabilities for continous improvement.
• Health Equity - driving the health equity agenda with life sciences organisation through identifying points of differentiation and embedding capabilities e.g. diversity in clinical trial design and recruitment, improving evidence generation for subpopulation groups, improving access through awareness and health infrastructure.

3 years of experience as a clinical Pharmacist at an oncology hospital, key responsibilities:

• Worked closely with clinical teams on the ward to monitor and advice on drug interactions and adverse effects
• Responsible for designing clinical trial prescribing ‘proformas’ in line with multiple clinical trial protocols
• Responsible for screening chemotherapy dosage, blood results and side effects in line with treatment guidelines. This includes compliance with clinical trial protocols
• Responsible for assuring the quality of Cytotoxic drug production from the aseptic unit
• Responsible for conducting clinical audits e.g. around drug wastage, patient compliance
• Responsible for providing Medical Information to both professional and public stakeholders via the Med-Info helpline, and detecting potential drug related adverse events