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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 Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative ..
... Quality Plans, etc., to ensure regulatory and past inspection commitments are ... knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, ... Clinical Development Communications and Public..
SENIOR REGULATORY AFFAIRS SPECIALIST - INTERNATIONAL Join us in ... and Geographies. Those working within Regulatory Affairs have direct impact on Medtronics ... That Change Lives The Senior Regulatory Affairs..
Job Description Testimonials Who We Are Culture Job Type: Full time Job Level: Senior Travel: Minimal (if any) At Takeda, we strive to provide transformational opportunities for every member of our ..
... Lives** The Senior Clinical Research Specialist (Sr. CRS) facilitates the development of ... compliance with applicable clinical and regulatory standards and in alignment with ... project teams, development, and..
... as a Senior Clinical Research Specialist (CRS), you will have primary ... products and to satisfy applicable regulatory standards and Medtronic internal requirements ... Clinical Management to satisfy applicable..
SENIOR REGULATORY AFFAIRS SPECIALIST Aortic Business Unit The Aortic ... that Change Lives The Senior Regulatory Affairs Specialist is responsible for developing strategies ... existing products, provide advice on regulatory..
... release deployments Ensure compliance with regulatory requirements/controls related to business systems ... Clinical Development Communications and Public Affairs Contingent Workers Data Sciences Engineering ... Legal Manufacturing Sciences Manufacturing/Production Medical..
... resolution of safety questions from regulatory authorities, investigators, internal development teams, ... operations, translational research, clinical pharmacology, regulatory affairs, quality assurance, biostatistics, data management, ... of safety input to..
... project teams as a pharmacovigilance specialist, ensuring the medical safety for ... Core Teams and Global Medical Affairs Core Medical Teams as the ... Medical Teams as the pharmacovigilance..
... hiring for multiple Research / Regulatory professionals across their program. CRS ... 1-3 clinical trials. We provide regulatory, clinical, and quality assurance services ... Clinical Research experience is required..
Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
... lives. SummaryThe Senior Manager supports Regulatory leadership in the development and ... of global nonclinical / clinical regulatory strategies through a programu2019s lifecycle.u00A0 ... interactions and the oversight of..
**SENIOR REGULATORY AFFAIRS SPECIALIST** Our vision is to become ... that Change Lives** The **Senior Regulatory Affairs Specialist** is responsible for managing regulatory submission activities for product maintenance ... Life**..
BioMarinu2019s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that ..
