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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?1/10/2016 Boston, MA Save This Job
Job Details Level Experienced Job Location USA-AZ-Scottsdale Position Type Full Time Job Shift Day Education Level 4 Year Degree Job Category Research Description POSITION SUMMARY The Clinical Operations Manager plays an essential role in the development and implementation of12/26/2015 Scottsdale, AZ Save This Job
Description/Job Summary MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 200+ dedicated individuals is advancing a pipeline of product candidates to treat patients with12/12/2015 Rockville, MD 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 an2/9/2016 Pleasanton, CA Save This Job
Company Overview Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the gastrointestinal tract. The12/30/2015 Redwood City, CA Save This Job
About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel therapeutic candidates that regulate cellular growth and repair. The company is a leader in understanding the biology of the12/13/2015 Cambridge, MA Save This Job
Regulatory Affairs Project Manager Location:Audubon, PA Job Code:RAPMCK0314 Description The Regulatory Affairs Project Manager assists in writing, submitting and gaining approval of 510(k) and IDE/PMA submissions to the Food and Drug administration (FDA) for class II and class1/5/2016 Audubon, PA Save This Job
JOB DESCRIPTION: The Sr. Clinical Research Associate will support the Director of Clinical Affairs in the management of clinical trials associated with the Clarity system. Several clinical trials are expected to be initiated in the coming year, and all clinical management2/4/2016 Alameda, 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, a12/30/2015 Redwood City, CA Save This Job
Job ID87 OverviewResponsible for independently developing regulatory strategy and filings (e.g. Annual Reports, Supplements, CBEs (Changes Being Effected), Protocols, etc.), providing critical review of CMC (Chemistry, Manufacturing, and Controls) and clinical submissions,12/22/2015 Blue Ash, OH Save This Job
About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the Transforming Growth12/13/2015 Cambridge, MA Save This Job
Req Id 2903 - Posted 12/23/2015 - United States - Massachusetts - Cambridge - Regulatory Affairs Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The Senior Quality Assurance Audit Manager is responsible for oversight1/5/2016 Cambridge, MA Save This Job
Req Id 2742 - Posted 12/23/2015 - United States - Massachusetts - Cambridge - Regulatory Affairs Job Description Print Preview The Senior Manager, Regulatory Affairs (Operations) will be responsible for overseeing operational aspects of all Aegerion regulatory submissions,2/4/2016 Cambridge, MA Save This Job
JOB DESCRIPTION GENERAL INFORMATION Position Title: Manager/Director, Regulatory Affairs Department: Regulatory Reports to: Vice President, Regulatory & QA FLSA Status: Exempt Version: 7/24/15 PURPOSE OF THE JOB Manage and direct the company?s global regulatory submissions1/4/2016 Fremont, CA Save This Job
ID 2016-1020 # of Openings 1 Job Locations US-MD Posted Date 2/4/2016 Category Other More information about this job: Overview: Leads and drives Quality System function and associated activities Proactively provides guidance to the functional teams to ensure Quality System2/8/2016 Baltimore, MD Save This Job