Associate Director, Clinical Research Physician, Neuroscience

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsAssociate Director, Clinical Research Physician, NeuroscienceShanghai - CN No longer accepting applications.Job IDR1604253Date posted07/07/2026DepartmentImmunology + FibrosisPosition Summary / ObjectiveThe Associate Director, Clinical Research Physician drives clinical strategy, and the design, execution, and interpretation of studies to ensure scientific inputs and high quality of delivery for early and late development projects in China.Serves as a primary source of medical accountability and oversight for multiple clinical trialsManages Phase I/II/III studies, with demonstrated decision making capabilitiesProvides medical and scientific expertise to cross-functional BMS colleaguesMaintains matrix management responsibilities across internal and external networksPosition ResponsibilitiesMedical MonitoringServe as an independent Medical Monitor for clinical trials byArticulating clinical development strategyAnalyzing, interpreting, and acting on clinical trial data to support developmentServing as principal functional author for Regulatory submission, study reports, and publicationsContributes to and is a key member of a high performing Study Team (ST) and a member of the China Development Team (DT)Provides input into protocols, contributing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations)Provides oversight and medical accountability for multiple trials across development clinical lifecycleLeads medical data review of trial data, including eligibility reviewHolds responsibility for site interactions in partnership with global clinical trial physician and/or clinical scientist for medical questions and education (including safety management guidelines)Assesses key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees contributions to safety narrativesFulfills GCP and compliance obligations for clinical conduct and maintains all required trainingClinical Development Expertise & StrategyEnsure clinical development activities are addressed with aligned strategies in close collaboration with cross function teamProvide inputs into clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets, in collaboration with China Development TeamSet up disease area strategy for clinical development activities in China, including but not limit to China-led study/indication (e.g. early signal detection) and major patient and investigator contribution in MRCT, to ensure development/study readiness in China from unmet needs, clinical capability, and competitor practice, and trial methodology perspective, with continuously update of knowledge and intelligence of designated disease area.Maintain direct contact and develop strong peer-to-peer scientific partnerships with external clinical experts to gather insights and input on disease area information.Explore collaborative connections with external China experts in academic/scientific database, patient cohorts, as well as real-world research to get insights on...