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Product Supply Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of5/28/2015 Cambridge, MA Save This Job
Job Code: 15-485 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor?s or Master?s degree in the life sciences preferred, plus relevant work experience required. Minimum of 7 years pharmaceutical/biotech research experience with at least 34/7/2015 Rockville, MD Save This Job
The Clinical Quality Assurance (CQA) Auditor is responsible for the development, enhancement and/or maintenance of CQA systems, under the direction of the Director, Quality Systems. Develops audit plans to ensure all clinical trials are conducted in compliance with the study4/27/2015 Cranbury, NJ 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 Growth5/11/2015 Cambridge, MA Save This Job
Job Title: Manager/Senior Manager, Quality Assurance Job Description: Quanterix is an exciting early stage company whose mission is to commercialize a game-changing instrument platform with a menu of immunoassay products that combines proprietary single-molecule sensitivity,4/29/2015 Lexington, MA Save This Job
Medsphere Systems Corporation, the leading provider of affordable and interoperable healthcare IT platform solutions, seeks a talented Clinical Product Manager: Pharmacy with a strong clinical background to join our growing team. Medsphere is a privately held company with4/13/2015 San Francisco, CA Save This Job
Department: Clinical Operations Job Location: South San Francisco, CA The Sr. Clinical Research Associate will participate in the activities associated with the evaluation, initiation, management and close-out of the Company?s oncology clinical trials. The Sr. CRA role requires5/15/2015 South San Francisco, CA Save This Job
Reports to: Senior Director, Manufacturing and Non-Clinical Operations Job Code: 2015 -70-4 Job Summary The Senior Manager, Pharmaceutical Process Development and Clinical Manufacturing manages the transfer and scale-up of synthetic chemical processes and sterile drug product5/13/2015 Gaithersburg, MD Save This Job
DESCRIPTIONJOB SUMMARY: This position will be a key member of the clinical team supporting accurate and timely processing of Home Sleep Studies, Patient Education and CPAP Titration Studies. This position will support the Clinical Operations Staff and other departments as4/21/2015 Glen Burnie, MD Save This Job
QA Compliance Specialist - Supplier QA/Materials QA Quality Assurance Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of4/28/2015 Cambridge, MA Save This Job
Job Location: San Francisco, CA Description: Supply Chain Associates are tasked with providing support to managers in transferring the Clinical Trial Material (CTM) from manufacturers to the Clinical Research Organization (CRO) and sites. The successful incumbent will plan and4/15/2015 San Francisco, CA Save This Job
Cleveland HeartLab, Inc. (CHL) is a premier next-generation clinical reference laboratory committed to advancing cardiovascular risk assessment through unique and proprietary diagnostic tests. We focus on novel inflammatory and cardiovascular biomarker technologies that allow for4/28/2015 Cleveland, OH Save This Job
Tracking Code 29-093 Job Description The Regulatory Affairs Specialist must be a talented and highly motivated individual. The position will participate in quality audits and support on-going compliance in the product development process. The position will assist in the4/5/2015 Lexington, MA Save This Job
Menlo Park, CA Major Responsibilities This position is primarily responsible for Quality Assurance activities to support R&D development projects - including clinical and preclinical studies. This position will mainly be focused in supporting cGMP activities and projects and may5/14/2015 Menlo Park, CA Save This Job
Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems4/28/2015 Cambridge, MA Save This Job
Qualifications: BS/BA degree in engineering or related field required, with 3+ years relevant work experience and in-depth knowledge of system development principles, concepts, and theories. Proven experience in developing and supporting laboratory automation for use in a4/27/2015 Alameda, CA Save This Job
JOB DESCRIPTION: Casenet is looking for a Business Analyst with experience in healthcare or insurance setting. Job responsibilities include: Facilitate meetings with business representatives, subject matter experts, analysts and developers Collaborate with business sponsors and4/13/2015 Bedford, MA Save This Job
Position Overview This is an Agile Scrum Product Owner position, reporting to the Product Manager for Integrations. As a Product Owner for Integrations you will be joining experienced Scrum teams: our Core Teams, who focus on Clarity LIMS; our Integrations Team, who focus on3/25/2015 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, a5/26/2015 Redwood City, CA Save This Job
Responsibilities Develop, review and revise the Quality Management System Direct the development and implementation of training on new / enhanced SOP management processes Direct Quality investigations and CAPA process Develop, review and revise Standard Operating Procedures,4/18/2015 King of Prussia, PA Save This Job