Min Wang work email
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Min Wang personal email
Bilingual MD with specialty in Internal Medicine. Twenty-five years of pharmaceutical/vaccine industry experience: drug/vaccine safety and global pharma R&D. Interests: global/international pharmaceutical/biotech activities related to drug/vaccine safety, clinical development, medical and regulatory affairs. Focus on North Americas and Asia.
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Global Head Of PharmacovigilanceFosun Pharma Mar 2022 - PresentShanghai, Shanghai, CnLead, structure, oversee, and direct all aspects of PV department and risk benefit management activities for Fosun developmental products across the different phases of the clinical trials as well as marketed products globallyMonitor industry best practices and trends in global safety regulations and guidelines. Recommends modifications and upgrades to existing departmental policies, and SOPs to ensure global regulatory complianceCollaborate and communicate safety related topics/strategies with other functional areas such Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Marketing, Manufacturing, and legalProvide functional leadership, strategic thinking, and effective coaching/mentoring to the Medical Safety stuffs to cultivate future PV leaders -
Global Medical Safety Physician - Vaccine TaJohnson & Johnson Jun 2013 - Feb 2022New Brunswick, Nj, UsProvide medical expertise and leadership to the GMS Vaccine TA and provide medical oversight to non-physician GMS staffProvide end-to-end (Phase 1 through product life cycle) safety support and surveillance Chair a multidisciplinary Safety Management Teams (SMT) with responsibilities include safety surveillance (including signal detection) and risk management activities (including Risk Management Plan (RMP) and Risk Evaluation and Mitigation Strategy (REMS), as well as activities related to managing the safety profile of assigned products Participate and provide strategic leadership on TA Clinical Development Teams (CDTs) and Clinical Teams (CTs) Participate and provide strategic leadership in HA interactions regarding safety and risk management, both written and verbal Provide strategic input and review to key regulatory or clinical documents, to ensure these key safety documents are of high medical and scientific qualityWork across the GMS TAs to align and improve common processes including providing strong leadership and a harmonized approach across clinical teams for safety data collection, assessment, and safety-related processes and issuesAssist in the creation, review and implementation of new SOPs, Work Instructions, guidelines, documents and other tools pertaining to safety assessment and risk management Participate on due diligence teams to evaluate Licensing & Acquisition opportunities -
Director, Product Safety OfficerSanofi Pasteur Jun 2010 - Jun 2013Paris, France, FrMonitor safety profiles of a portfolio for investigational and marketed products by leading safety management team/safety evaluation team, detecting and evaluating safety signals, and generating risk management plans (e.g., RMP, PVP and REMS); Identify any important identified risks, potential risks and important missing safety information that should be brought to the attention of the Global Labeling group; Contribute to safety sections in key regulatory and clinical documents as related to clinical development (e.g., CSRS, IBs, ASRs/DSURs, CDSs); Accountable for compiling safety-related regulatory documents (e.g., PSUR/PBRER) and responding to ongoing inquiries from regulatory authorities and health professionals in a timely manner. -
Medical Safety OfficerSanofi Pasteur Feb 2008 - Jun 2010Paris, France, FrEvaluated safety profiles of assigned marketed products (prescription drugs and medical devices) by assessing early safety signals from post-marketing reports of ADRs and product technical complaints leading to AEs and conducting evaluation of those potential safety signals; Contributed to joint team decisions on study proposals and protocols, responses to regulatory authorities, updated labeling, and other cross-functional Medical Affairs activities; Contributed to the development of risk management strategies, RMPs, and related implementation/communication plans for assigned registered/marketed products
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BioinformaticianSanofi Pasteur Jul 1999 - Jan 2008Paris, France, FrGlobal pharmaceutical R&D
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Senior ScientistGlaxosmithkline Feb 1997 - Jul 1999Brentford, Middlesex, GbGlobal pharmaceutical R&D
Min Wang Skills
Min Wang Education Details
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Shanghai Medical UniversityToxicology And Epidemiology -
Shanghai Medical UniversityInternal Medicine
Frequently Asked Questions about Min Wang
What company does Min Wang work for?
Min Wang works for Fosun Pharma
What is Min Wang's role at the current company?
Min Wang's current role is Global Head of Pharmacovigilance.
What is Min Wang's email address?
Min Wang's email address is mi****@****jnj.com
What schools did Min Wang attend?
Min Wang attended Shanghai Medical University, Shanghai Medical University.
What skills is Min Wang known for?
Min Wang has skills like Pharmacovigilance, Vaccines, Regulatory Affairs, Oncology, Infectious Diseases, Immunology, Pharmaceuticals, Pharmaceutical Industry, Medical Affairs, Bioinformatics, Clinical Development, Lifesciences.
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