Clinical Regulatory Document Specialist Jobs in Princeton

... and/or group supervision to Behavioral Specialist Consultants and Mobile Therapists. Assisting ... The position directly interfaces with clinical staff in the form of ... psychological services through consultation with..

... content to organizations such as clinical practice guidelines, compendia, and HTA) ... guidelines, compendia, and HTA) per clinical development program, publications, data presentations, ... of medical integrity, accuracy and..

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 ..

... and the preparation of the clinical trial applications (CTAp) for programs ... updates at program level. The specialist will gain expertise to progressively ... and tracking of the core..

... looking for a dynamic Quality Specialist I to join our dedicated ... excellence in their work.nThe Quality Specialist I will work within the ... SOP, and documentation standards. Performs..

... 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:..

... results. Senior Scientific Writer - Clinical Study Protocols, Immuno‑Oncology and/or Specialty ... Specialty Position Objective: To author clinical study protocols and other related ... study protocols and other related..

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 ..

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),..

... content to organizations such as clinical practice guidelines, compendia, and HTA) ... guidelines, compendia, and HTA) per clinical development program, publications, data presentations, ... of medical integrity, accuracy and..

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 ..

Summary Provides regulatory guidance that shapes the direction ... direction of BMS teams (e.g., Regulatory Team, Multi functional Development team, ... Recognized as a Leader in Regulatory Science and credible..

... of the progress of a clinical trial, and of ensuring that ... Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable ... Practice (GCP), and the applicable..

... and ensuring compliance with global regulatory requirements. Summary: The function of ... identify and report ESRs within regulatory agency timelines worldwide. Prepares high-quality ... current, and is submitted within..

... SDTM Programming lead for all regulatory submissions Expertise in SDTM automation ... SDTM datasets to ensure meets regulatory compliance Provide input to the ... to the design of the..

... content to organizations such as clinical practice guidelines, compendia, and HTA) ... guidelines, compendia, and HTA) per clinical development program, publications, data presentations, ... of medical integrity, accuracy and..

... identify and report ESRs within regulatory agency timelines worldwide. Responsibilities Prepares ... current, and is submitted within regulatory timelines. Participates in the evaluation ... event reports from spontaneous reports,..

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 ..