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Job Details Regulatory Affairs Manager (001121) Job Number:001121 Job Title:Regulatory Affairs Manager Number of Openings:1 Job Type (Employment Type):Direct Hire Country:United States State/Province:California City:San Diego Job Schedule:Full Time Level of Education:Bachelor's4/24/2016 San Diego, CA Save This Job
Job Description The Clinical Trial Manager in collaboration with the Clinical Project Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities?4/23/2016 Boston, MA Save This Job
Clinical Operations Cambridge, MA, United States Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and engineering, Merrimack aims to6/21/2016 Cambridge, MA Save This Job
Product Supply Cambridge, MA, United States We are looking for a talented Clinical Supply Manager to join our team in Cambridge! Job Responsibilities: Work closely with Clinical Operations to monitor and track clinical trial enrollment plans and actual enrollment Collaborate5/22/2016 Cambridge, MA Save This Job
Location:Pleasanton, California DESCRIPTION Summary: Provide medical information and clinical support in post-market commercial use and continued learning of ZELTIQ products. Responsible for the operation of the Clinical Outcome Support group. To facilitate and maintain an4/24/2016 Pleasanton, CA Save This Job
Position Summary The Manager of Regulatory Affairs is accountable for the preparation and management of simple and complex regulatory submissions. They will act as liaison between Regulatory Affairs and other functional areas on various projects including external CROs, partners,5/26/2016 Cambridge, MA Save This Job
Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.6/22/2016 Audubon, PA Save This Job
Manager - Regulatory Affairs (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Manager positions will be responsible for administering the day-to-day Regulatory Affairs operations. Responsibilities may include: Directly or indirectly managing6/15/2016 Westborough, MA Save This Job
COMPLIANCE Department: Finance Job Location: South San Francisco Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators as potential treatments for debilitating diseases in which muscle5/9/2016 South San Francisco, CA Save This Job
Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a5/17/2016 Redwood City, CA Save This Job
Helomics is a bio-technology company located on the South Side of Pittsburgh. Helomics assists oncologists and surgeons in choosing effective cancer therapies for their patients. As leaders in the science of individualizing cancer therapy through the use of a proprietary and5/10/2016 Pittsburgh, PA Save This Job
Department: Regulatory Affairs and Quality Assurance Hiring Manager: Director of Regulatory Affairs Summary of Position: Under the direction of the Director of Quality Assurance, the Manager/Associate Director GMP QA is responsible for providing QA and Technical support to6/6/2016 Boston, MA Save This Job
This newly created position reports to the Director, Quality Assurance Compliance and is responsible for assuring GCP compliance with Alder SOPs, ICH and FDA/EMA regulations. Specific responsibilities will include: Provide GCP compliance support: participate in Clinical Project6/24/2016 Bothell, WA Save This Job
This position will report to the Vice President of Commercial Strategy who overseas New Product Marketing, Market Research, Forecasting, Analytics and Competitive Intelligence functions for the company. The role will be primarily responsible for forecasting Alder?s lead5/25/2016 Bothell, WA Save This Job
This newly created position will work closely with the VP Program & Portfolio Management (PM) to provide specialized cross-functional PM leadership for Alder?s drug development programs through expert planning, risk mitigation and execution. Collaborates with functional project5/25/2016 Bothell, WA Save This Job
Career Opportunities: Rare Disease Manager - NY Metro (3541) Req Id 3541 - Posted 06/15/2016 - United States - New York - New York City - Sales The field based Rare Disease Manager will be responsible for preparing the market, educating customers and ultimately performing6/22/2016 New York, NY Save This Job
Req Id 3621 - Posted 05/05/2016 - United States - New Jersey - Newark - Sales ? Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The field based Rare Disease Manager will be responsible for preparing the market,6/22/2016 Newark, NJ Save This Job
Location:Audubon, PA Job Code:RAGJ0316 Description The Research Assistant will be responsible for conducting post marketing clinical research on Globus Medical products. The candidate should have demonstrated abilities to conduct clinical studies and work with product5/23/2016 Audubon, PA Save This Job
inShare Location: Blue Ash, OH Aprecia is a specialty pharmaceutical company committed to transforming customers' experience with highly prescribed high-dose medications. Built upon our proprietary three-dimensional printing (3DP) technology platform, we develop and6/7/2016 Blue Ash, OH Save This Job