Daniel Chew
Founder @Haven Consulting
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WORK HISTORY
Founder @Haven Consulting
Supporting Life Sciences, MedTech and Neurotech businesses through consultancy services
EDUCATION
Queen Mary University of London
PhD, Neuroscience
University of Cambridge
Post Doctorate, Neurobiology and Neurosciences
University of Bristol
BSc, Neuroscience
SKILLS
ABOUT DANIEL CHEW
EXECUTIVE SUMMARY I am an experienced scientific innovator and thought leader with over 20 years of scientific development in Neuroscience, Immunology, and Metabolic biology authored in over 40 manuscripts and 15 patents. I have spearheaded the roadmaps of high-impact translational programmes and teams, delivering cutting-edge innovation across multiple immune-inflammation and metabolic indications. I have over 13 years of experience in leading Industrial Life Science treatment concept ideation, through to clinical trial execution. Having served as Senior Director in Galvani Bioelectronics, a GlaxoSmithKline and Alphabet joint venture, I delivered strategic scientific leadership across the R&D landscape, including the end-to-end development of Class active implantable treatments across multiple indications into the clinic. I deliver this expertise through matrixed and direct line team leadership, multi-million-pound budgeted accountancy, with regulatory quality and risk-management oversight.CORE EXPERTISEDelivery – Coordination and execution of R&D programme portfolio | Scientific ownership of asset from concept ideation through to clinical translation | Expertise in anatomy, surgery, biology, pharmacology | Preclinical and clinical strategy and protocol design | Regulatory documentation and submission | Scientific publication and patent generation | Clinical trial execution | Agile Programme Management | GLP, GMP, ISO and SOP standard processes | Fail-Fast data driven decision making. Leadership – R&D platform and programme development leadership | Cross-functional matrixed and line management of 20 individuals | Accountable for multi-million-pound budget | External and internal stakeholder management | C-suite level reporting | Contract negotiation | Medicines Vision and Target Medicines Profile | Strategic partnership development | Patient and Public Customer analysis and Informed Consent | Scientific, Safety and Data Advisory Review boards | Quality and Risk management and design control | Animal and human tissue ethical frame working.
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