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Job Information Bristol Myers Squibb Clinical Trial Result Specialist in Princeton New Jersey Bristol-Myers ... their personal lives. Description The Clinical Trial Results Reporting Specialist is responsible for creation of..
... The CAR T Cell Therapy Clinical Specialist (CTCS) will serve as a ... treatment site teams participating in clinical trials or administering chimeric antigen ... training to appropriate personnel..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... in their personal lives. GDO Clinical Trial Planning Specialists are responsible ... for building and tracking of clinical trial execution plans (phase I-IV) ... Microsoft Project) for Phase I-IV..
... and transformative business results. Global Clinical Trial-Submission Unit (GCT-SU) Specialist: This role has two key ... 1) Provide support to Senior specialist in CTAp preparation activities 2) ... Authorities:..
Job Information Bristol Myers Squibb Clinical Trial Monitor/Clinical Research in Princeton New Jersey ... of the progress of a clinical trial, and of ensuring that ... Standard Operating Procedures (SOPs),..
... maintenance and Implementation of BMS clinical data Standards Participate in the ... development and maintenance of global clinical data standards, including operational (eCRF ... Data Model (ADaM) standards, and..
... Bristol Myers Squibb Associate Director, Clinical Operations in Princeton New Jersey ... a cross functional or functional Clinical Operations Unit, ensuring execution to ... Operations Unit, ensuring execution to..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and ..
... innovation and transformative business results. Clinical Supply Operations Specialist will lead the manufacture of ... policies and procedures. In addition, Specialist will be responsible for leading ... of formulae..
... Research and Development (R&D), Global Clinical Operations (GCO), Global Data Management ... Centralized Monitoring is responsible for clinical trial data acquisition, quality review, ... Summary / Objective The Global..
... to the design of the clinical trial database from an SDTM ... plus years of experience supporting clinical trials for regulatory submissions Experience ... SDTM deliverables Thorough understanding of..
... Position Summary / Objective The Clinical Data Standards Manager is a ... and sustainability of the Global Clinical Data Standards, compliant submissions and ... the consistent implementation of global..
... transformative business results. Job Title Clinical Trial Disclosure Specialist (D5) Division Research & Development ... Global Development Operations / Global Clinical Compliance & Continuous Improvement / ... & Continuous..
... of the progress of a clinical trial, and of ensuring that ... Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable ... Monitor (MM), Protocol Manager (PTM),..
... Where you Come In The Pharmacy Special Investigations Professional is responsible ... degree Minimum 2 years of pharmacy fraud investigations and/or pharmacy auditing and/or pharmacy tech experience Advanced knowledge..
Job Information Humana Pharmacy Special Investigations Professional (Fraud, Waste ... Where you Come In The Pharmacy Special Investigations Professional is responsible ... degree Minimum 2 years of pharmacy fraud investigations..
... make a difference. The Manager, Clinical Data Standards, will manage the ... the consistent implementation of global clinical data standards for BMS projects ... and maintenance of BMS's global..
... business results. Training & Development Specialist The Training & Development Specialist is responsible for the successful ... site Manufacturing Training Program. The Specialist assists in determining training solutions .....