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ROLE SUMMARY Lead a team of in vivo pharmacologists developing and implementing disease models for the mechanistic characterization and evaluation of novel anticancer therapeutics. This team will provide a critical..
Associate Director of Analytics Field Sales - Hematology/Oncology in Summit New Jersey Description Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer,..
Senior Director Strategy Development & Analytics in New York New York ROLE SUMMARY Reporting to the Vice President of Strategy development for Pfizer Global Supply (PGS) The Senior Director Strategy..
Clinical Research Associate - • Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical..
Clinical Research Scientist The incumbent is responsible for, but not limited to the following: • Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies • Prepare..
Pharmacy Manager Show me jobs like this one Job Ref: 677430BR Employer: CVS Health City: New York State: New York (NY) Position type: Full-Time Position Summary: Summary: Health is everything...
Staff Pharmacist FT Show me jobs like this one Job Ref: 677432BR Employer: CVS Health City: New York State: New York (NY) Position type: Full-Time Position Summary: Summary: Health is..
The Oncology Clinical Content Associate/Manager will be responsible for the development and maintenance of medical content, and for helping to integrate this content into Flatiron’s technology platform to make it..
Responsibilities: The incumbent is responsible for, but not limited to the following: • Assist in the management of the day to day operations of clinical trials including coordination and oversight..
Come to an industry leader where you will support the Head Legal of the Biologics Technical Development and Manufacturing Operations (“BTDM”) in the management of all legal matters in scope..
Come to an industry leader where you will manage the stability program to ensure the compliant and timely design, interpretation and reporting of stability studies for pharmaceutical drug products as..
Respiratory Business Specialist - Jersey City, NJ','179501','!*!Description: The Respiratory Business Specialist is responsible for developing and implementing a plan for maximizing net sales of BIPI and co-promoted respiratory products..
Qualifications Bachelor's degree in business or related analytics or supply/operations Experience in clinical operations function within pharmaceutical, biotech, clinical research, or related environment is preferred Microsoft Word, Excel, PowerPoint, Project..
Qualifications 10 yrs experience in the pharmaceutical industry with 7 yrs experience in drug development, clinical supply chain management and/or clinical manufacturing and 3 years in compliance management Experience in..
Senior Clinical Research Associate, Early Stage-New York-CLI006263 DESCRIPTION Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader..
nSolid Organ Transplant Clinical Pharmacy Specialist needed for a large teaching hospital in NYC with one of the most active and successful transplant programs in the country. This pharmacist..
Clinical Research Associate (CRA) The Company: Global Pharmaceutical Company is seeking to hire a Clinical Research Associate (CRA) for a one year contract at their New Jersey headquarters. The CRA..
Pharmacy Manager in TETERBORO New Jersey 882408BRReq ID:882408BRCompany Summary:What started small, with a single discount store and the simple idea of selling more for less, has grown over the last..
Qualifications Bachelor Degree in health or biologic science (BS/BA/ BScN or higher) is required; masters-level degree is preferred A minimum of 5 years clinical study management experience in biopharmaceutical industry,..
Qualifications Must have 7-9 years of pharmaceutical industry experience in manufacturing, pharmaceutical development or QA, with a minimum of 5 years of Biologic Regulatory CMC experience, including the preparation of..
Qualifications Pharm.D. or Ph.D. in a pharmaceutical science preferred RPh or RN with previous pharmaceutical industry-based Drug Information experience considered 1-3 years of Drug Information, Medical Writing or Medical/Promotional review..
New York , NY , United States Manage forecasting and managing budgets for data management (DM) Strategic vendors within specified parameters oversee DM strategic vendor performance (metrics timelines budgets resources..
Global Clinical Leader Thrombosis MD in Parsippany New Jersey Your tasks and responsibilities The Global Clinical Development Leader will be responsible for strategic (phase II-III) and operational clinical development activities..
Medical Affairs Graduate Scholar in Whippany New Jersey Your tasks and responsibilities The Medical Affairs Graduate Scholar position will allow someone who has completed advanced studies in a science or..
As the Associate Director of Strategy & Operations for the Solid Tumors Franchise, the candidate will sit at the intersection of the brands and the Director of Strategy & Operations..
Job Purpose The Associate Clinical Development Director (Assoc. CDD) is responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. May be..