Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and
Basic purpose of the job* The Head of Development Regulatory Affairs 1 or 2 has responsibility to develop and implement regulatory strategy for the assigned therapeutic areas (TAs) and exercises activities which include: Guide subordinates on
Basic purpose of the job Delivers project management support to the asset team and next–level teams with the focus on asset strategy execution and asset progress. Coordinates the interactions with all key stakeholders, local and Global
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon
Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the
Publication Strategy Manager パブリケーションストラテジーマネージャー Basic purpose of this job: 各疾患領域の戦略に沿った、研究データの適切適時なパブリケーション（論文公表・学会発表）を推進する役割です。 To define and execute the local publication plans in a strategic and compliant manner, considering the overarching HPBU and brand specific strategy and ensuring: - regular
Job Description SummaryThe SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies in
Job Opportunity: Pharmacovigilance Associate - Japan, Osaka About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation and excellence, and they welcome
Job Opportunity: Clinical Research Associate I (CRA I) - Japan, Tokyo (Hybrid: Office/Remote) About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation
About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes you to join its mission to shape the future of
Job Opportunity: Senior Biostatistician Responsibilities * Ensuring that all statistical aspects of documentation pertaining to clinical programs and non-study activities meet required standards and are statistically accurate. * Influencing study design and analysis, and defending statistical approaches internally
Job Opportunity: Project Manager, Laboratory - Japan, Tokyo (Hybrid: Office/Remote) About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines
Key Accountabilities Country Quality System management Lead the implementation and maintenance of GxP quality system with respective operation units, the continues quality system implementation for competencies and related Quality documentation of GxP area: medical, pharmacovigilance, regulatory and
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon
Job Description SummaryAccountable for the oversight and coordination of program and study level (re-)feasibility assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes, GCP, ICH and regulatory requirements.
Basic purpose of the job Based on sound medical knowledge, this role defines the local Patient Safety & Pharmacovigilance (PSPV) strategy not aonly for the delegated asset (AT) but also other products as needed and ensures
