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Job Description COMPANY SUMMARY:At Intercept, our mission is to build a healthier tomorrow for patients with progressive non-viral liver diseases. Intercept's lead product, obeticholic acid (OCA), is a first-in-class farnesoid X ..
Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies outsourced ..
The Director of Robotics and Business Process Automation is a key member of the Application Management services and delivery organization, responsible for planning and driving the execution of automation projects. The ..
Developing innovative therapies is one of the most challenging, most essential and personally rewarding fields in science. This is the most exciting time to be a part of Astellas, a company ..
Clinical Outcome Assessment (COA) Specialist is responsible for working directly with COA Manager to provide technical and general administrative support for assigned eCOA studies including but not limited to; managing and ..
We are currently looking to fill a Manufacturing Project Specialist – Manufacturing Execution and Manufacturing Systems position with a 1st shift, Monday-Friday, 8:00am-4:30pm schedule. Regeneron successfully manufactures a range of biopharmaceuticals ..
ROLE SUMMARYrnrnVaccines is the only place in Pfizer where you can contribute to patients in a way like no other – you can prevent sickness and disease. This is at the ..
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 Company ..
We are currently looking to fill an Associate Manager of QA Microbiology. This position manages a team for microbiologically based initiatives. Aspects of training, investigation activities, project implementation, data collection, and ..
The Pre-Clinical Research Study Coordinator will work in collaboration with Therapeutic Focus Area (TFA) teams by providing logistical support for outsourced pre-clinical pharmacology and proof of concept studies at Regeneron.As a ..
The Senior Director of Medical Affairs will fulfill an important strategic leadership role and has high visibility in the organization, reporting into the Executive Director of Medical Affairs. He/she will spearhead ..
We are seeking a Temp-Scientist to support key formulation and drug product development activities within the Formulation Development Group of Regeneron Pharmaceutical Inc. at Tarrytown, NY.In this role, you will develop ..
Our Formulations Development Group (FDG) is looking for an enthusiastic Staff Scientist to work on the development of drug product formulations for a diverse set of modalities such as mAbs, mAb-like ..
**Careers that Change Lives** Bring your talents to an industry leader in medical technology and healthcare solutions were a market leader and growing every day. You can be proud to sell ..
Our Formulation Development Group (FDG) is seeking a Temp-Scientist, Analytical Formulation Development to support key analytical method development and method characterization activities in our Tarrytown, NY location.A Scientist is responsible for ..
The Clinical Biospecimen & Data Specifications Manager (CBDSM) role within Quality and Compliant Operations (QCO) is responsible for supporting the Vaccine Research & Development (VRD) Clinical Compliance Head and Research Informatics ..
We are looking for an Animal Research Associate to join the VelociGene team. This person would be responsible for various tasks associated with producing and maintaining our Tier1, corporate, and collaborator ..
Our client is seeking a Senior Project Manager with strong pharma experience needed for a long term remote contract. Budgeting and forecasting expertise Experience building project charters Familiarity facilitating UAT applications ..