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Job Summary The Otsuka US Legal Team is looking for an attorney familiar with the legal and regulatory frameworks within which life sciences companies operate. The attorney will provide proactive..
Job DescriptionnnNew hires in office-based roles in the US & Puerto Rico will be required, subject to applicable law, to demonstrate that they have been fully vaccinated for COVID-19 or..
Job DescriptionnnNew hires in office-based roles in the US & Puerto Rico will be required, subject to applicable law,u00a0to demonstrate that they have been fully vaccinated for COVID-19 or qualify..
The Clinical Research Associate is tasked with oversight of all research activities as they relate to the Adult Oncology and Internal Medicine divisions. This includes oversight of data management, protocol..
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..
Job Information Bristol Myers Squibb Clinical Trial Registration Specialist in Princeton New Jersey At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science...
ROLE SUMMARYThe Senior Medical Director will be responsible for leading several US Medical Affairs activities in support of Multiple Myeloma, including providing strategic leadership for clinical research and launch readiness...
We are seeking a dynamic, results-oriented professional to join the Duane Reade team as a drug clerk. This person must have open availability to work days, nights and weekends as..
NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have..
We are a world class manufacturer of industrial additives for the Coatings, Ink, Adhesive, Textile, Metalworking, Paper, Food and Building Products. We are an ISO 9001 & 14001 registered company..
The Director, Regulatory Labeling is responsible for leading one or more Regulatory Labeling Strategy Team Therapeutic Areas to develop and manage the processes for creation, maintenance, and archiving of the..
The Manager, Data Management- Clinical Data Standards creates and maintains global metadata repository by collaborating with clinical development line function representatives as part of Regeneron Data Governance model. Works with..
Job Description We are a world class manufacturer of industrial additives for the Coatings, Ink, Adhesive, Textile, Metalworking, Paper, Food and Building Products. We are an ISO 9001 & 14001..
Title: Method Validation Scientist nLocation: Monmouth Junction, NJ nSchedule: Monday - Friday nType: Direct Hire nStart date: ASAP n nResponsibilities: n n MV Scientists perform method validation studies to support..