Senior Manager, Medical Communications
Washington
5/20/2013 2:17 PM
We are currently seeking a Senior Manager, Medical Communications, to fill a permanent, full-time position leading the Medical Communications department within the Medical Affairs group at Seattle Genetics.
DUTIES & RESPONSIBILITIES:
Manage the activities of the Medical Communications department, including budgetary oversight and supervision of Medical Communications personnel. Develop corpor
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Associate Director Contract Manufacturing
Washington
5/9/2013 8:01 PM
The Contract Manufacturing Associate Director leads the process for small molecule manufacturing in support of commercial operations, and manages the Manufacturing of the commercial intermediate. In addition negotiates complex technical and financial supply agreements, develops and maintains supply and business relationships with commercial CMOs (Contract Manufacturing Organizations) and business
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Scientist, Protein Sciences
Washington
5/9/2013 7:59 PM
We are seeking an energetic, highly motivated, and creative protein engineer to join Seattle Genetics’ Protein Sciences group.
The successful candidate will:
• Lead and participate in efforts to further understand and improve our Antibody Drug Conjugate (ADC) platform
• Enhance protein biochemistry of our molecular targets
• Managerial experience is desirable.
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Drug Safety Specialist
Washington
4/29/2013 2:45 PM
Reporting to the Manager, Case Management, the Drug Safety Specialist has the primary responsibility for the preparation and timely submission of all safety reports, including expedited safety reports. Additional duties and responsibilities include:
• Receive, process, evaluate (from a regulatory standpoint) and report investigational and marketed safety information (e.g., adverse events, pregn
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Senior Research Associate - Preclinical
Washington
4/29/2013 1:54 PM
We are seeking an innovative research candidate to be on the forefront of evaluating novel antibody drug conjugates and other candidate therapeutics in our pipeline using in vivo cancer xenograft and syngeneic tumor models.
Responsibilities
Primary responsibilities include planning, coordinating and conducting studies in rodents to test experimental compounds for activity, pharmacologic mechan
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Pharmacovigilance (PV) Quality Manager
Washington-Bellevue/Redmond
4/26/2013 1:49 PM
Summary: Reporting to the Drug Safety Director, the PV Quality Manager is responsible for monitoring and assessing Drug Safety procedures to assure compliance with global regulatory requirements. This individual is also responsible for ensuring appropriate training for Drug Safety personnel.
This individual liaises with department management and cross-functional teams throughout the company
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Research Associate I/II, Cell Sciences
Washington
4/23/2013 1:55 PM
RA will work in a collaborative setting with other cell line and cell culture development staff on CMC development projects. RA’s primary responsibility is to support recombinant cell line and cell culture development. This will include recombinant protein productions, maintaining clinical and research cell lines, solution and cell culture media preparation, cell culture analytics, lab and instr
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