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Senior Product Manager / Associate Director Global Medical Marketing My client, a small, global, publicly traded biopharmaceutical company, based in CT (2 hours from Boston and 1 ½ hours from NYC) develops drugs that inhibit certain immune system functions that cause auto immune disorders, cancers, and other diseases. Their marketed product is for the treatment of a rare genetic blood disorder. Th...
Full job description at Monster
Posted Thu 12th January
Senior Product Manager / Associate Director US Marketing - Nephrology My client, a small, global, publicly traded biopharmaceutical company, based in CT (2 hours from Boston and 1 ½ hours from NYC) develops drugs that inhibit certain immune system functions that cause auto immune disorders, cancers, and other diseases. Their marketed product is for the treatment of a rare genetic blood disorder. T...
Full job description at Monster
Posted Thu 12th January
The Regulatory Affairs Scientist should have a practical and working knowledge of the FDA/ICH regulatory requirements for biotech-derived recombinant protein products to review and prepare timely, organized and scientific submissions to regulatory agencies. Position Responsibilities: · Involvement in short term and long term regulatory drug development and submission strategies for products in the...
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Posted Tue 24th January
As the only global provider of commercial solutions, Quintiles understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers, physicians and patients. A significant part of our business is acting as th...
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Posted Today
Senior Product Manager / Associate Director Global Marketing - Neprhology: My client, a small, global, publicly traded biopharmaceutical company, based in CT (2 hours from Boston and 1 ½ hours from NYC) develops drugs that inhibit certain immune system functions that cause auto immune disorders, cancers, and other diseases. Their marketed product is for the treatment of a rare genetic blood disord...
Full job description at Monster
Posted Thu 12th January
Associate Director / Director Global Marketing - AustralAsia - Small Specialty CT Pharma The Associate Director/Director Global Marketing Australasia will drive the commercial activities in the AustralAsia region for a novel orphan therapy in the global hematology and nephrology space. He/she will contribute to the development of the global marketing strategy and take a leading role in its impleme...
Full job description at Monster
Posted Thu 12th January
NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Clinical Site Manager Our client is developing leading positions in seven major therapeutic areas. Candidate must be flexible and dependable with a BA, BS or MS degree. •Successful candidate must have 3-5 years of clinical research experience, be capable of handling multiple projects ...
Full job description at Monster
Posted Fri 10th February
The Associate Director / Senior Product Manager Global Marketing, Nephrology as a member of the brand team will drive the global marketing of a novel orphan therapy in the nephrology space. He/she will contribute to the development of the global marketing strategy, support its implementation in all regions outside North America and be a key contact point with country marketing managers. Responsibi...
Full job description at Monster
Posted Today
The Director / Associate Director Global Marketing Australasia will drive the commercial activities in the Australasia region for Soliris, a novel orphan therapy in the global hematology and nephrology space . He/she will contribute to the development of the global marketing strategy and take a leading role in its implementation in the Australasia region. Responsibilty The candidate will serve as ...
Full job description at Monster
Posted Today
Clinical Trials Manager Overview: The Clinical Trials Manager works closely with internal team members and vendors to ensure that assigned clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and budgets. Position Responsibilities: · Comprehensive oversight of operational aspects of assigned clinical trials · Management...
Full job description at Monster
Posted Thu 2nd February
DNA Sequencing · Develop, validate, implement, and sustain robust analytical methods for incoming, in-process, and finished product release testing of critical instrumentation and reagents, including enzymes, nucleotides and buffers. · Work closely with R&D scientists (within 454 and Roche), external vendors, and the scientific community to understand the current state of the art in various analyt...
Full job description at Monster
Posted Mon 13th February
DNA Sequencing · Develop, validate, implement, and sustain robust analytical methods for incoming, in-process, and finished product release testing of critical instrumentation and reagents, including enzymes, nucleotides and buffers. · Work closely with R&D scientists (within 454 and Roche), external vendors, and the scientific community to understand the current state of the art in various analyt...
Full job description at Monster
Posted 3 days ago
Alexion Pharmaceuticals, Inc. is a biopharmaceutical company working to develop and deliver life-changing therapies for a wide array of serious and life-threatening medical conditions. These include hematologic and kidney diseases, transplant, other inflammatory disorders, and cancer. Alexion is both evaluating other potential indications for Soliris, it's first marketed product and pursuing the d...
Full job description at Monster
Posted 2 days ago
Company Description: Alexion Pharmaceuticals, Inc. is a biopharmaceutical company working to develop and deliver life-changing drug therapies for patients with serious and life-threatening medical conditions. Alexion is engaged in the discovery, development and commercialization of therapeutic products aimed at treating patients with a wide array of severe disease states, including hematologic and...
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Posted Today
The Sr. Manager/Associate Director, Global Medical Training at Alexion Pharmaceuticals, Inc. will support the strategic direction of the Global Medical Affairs group in the development and implementation of learning and leadership initiatives across the global medical affairs organizations. The Sr. Manager/Associate Director, Global Medical Training will: Build, implement and facilitate regularly ...
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Posted Today
Job Title: Associate Director, CMC Regulatory Affairs Department: Regulatory Affairs Job Code: Date Available: immediate Location: Alexion Pharmaceuticals, Inc. 352 Knotter Dr. Cheshire, CT 06410 United States www.alxn.com recruit@alxn.com fax: 203-699-9940 Responsibilities: Currently Reports to the SVP, Global Regulatory Affairs; subject to change. Provides the strategic guidance for worldwide CM...
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Posted Today
ALEXION PHARMACEUTICALS POSITION SUMMARY TITLE: Associate Director, Clinical Quality Assurance LOCATION: Cheshire, CT REPORTS TO: Senior Vice President, Global Quality and Compliance Company Description: Alexion Pharmaceuticals, Inc. is a biopharmaceutical company working to develop and deliver life-changing drug therapies for patients with serious and life-threatening medical conditions. Alexion ...
Full job description at Monster
Posted Today
New Haven is known for being the home of Yale University. Major manufacturing in New Haven includes clocks, watches, firearms, ammunition, paper and rubber products and textiles. The city is located where the Quinnipiac River enters Long Island South and the city serves as a major port for the petroleum industry. The city is known in history for being the site where the first commercial telephone exchange took place. New Haven has a rich historic district and is most noted by tourists for maintaining three churches that were built in the early part of the 19th century.
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