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Clinical Research Associate II Reports to: Clinical Trial Manager II Job Code: 2015-70-3 Job Summary The Clinical Research Associate II (CRA II) will provide in-house support for clinical trial operations including management of clinical trial sites and Contract Research3/2/2015 Gaithersburg, MD Save This Job
Job Location: San Francisco, CA Description: FibroGen seeks a highly motivated Senior Clinical Research Associate (Sr. CRA). This position focuses on Global Phase 3 study execution for the FibroGen anemia program and may also have responsibility for specific tasks including3/4/2015 San Francisco, CA Save This Job
Category: Clinical Research Company Description: Dicerna Pharmaceuticals is a biopharmaceutical company focused on the discovery and development of innovative treatments for rare inherited diseases involving the liver and for cancers that are genetically defined. Dicerna?s entire3/31/2015 Cambridge, MA Save This Job
Position Description The Clinical Project Manager will be responsible for overseeing day-to-day study operations of one or more clinical studies to meet individual clinical trial objectives and corporate goals. For clinical studies assigned, this individual is responsible for3/23/2015 Cambridge, MA Save This Job
Verastem is seeking a Clinical Trial Manager to be responsible for high quality and timely execution of clinical trials. Responsibilities Lead study team activities, coordinating internal and external resources along with CRO activities, from study startup through closeout. Work2/26/2015 Needham, MA Save This Job
Department: Clinical Development Job Title: Sr. Manager, Statistical Programming Job Location: San Diego, CA Description: The Statistical Programmer provides statistical programming technical leadership and support to team members including programming outputs (datasets,2/9/2015 San Diego, CA 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 class2/18/2015 Audubon, PA 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 TGF--- protein1/27/2015 Cambridge, MA Save This Job
Program Manager 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 the1/27/2015 Cambridge, MA 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, a3/16/2015 Redwood City, CA Save This Job
Department(s): Clinical and Regulatory Affairs Reports to: Chief Scientific Officer Company Prolacta is the pioneer in human milk-based nutritional products for premature infants in the neonatal intensive care unit (NICU). Prolacta believes that there is no adequate replacement2/23/2015 City of Industry, CA Save This Job
The Senior Project Manager is responsible for delivering the highest quality clinical trial data capture software & service with on-time delivery. The Senior Project Manager interfaces with clients as well as project teams. In addition, the Senior Project Manager provides1/25/2015 Boston, MA Save This Job
Job Code: 15-635 Location: Rockville, Maryland Applicants must meet the following requirements: Bachelor's Degree required Minimum 3 years of relevant experience in contracting, outsourcing or finance in the clinical trial space The selected candidate will be responsible2/25/2015 Rockville, MD Save This Job
Position Summary: The Clinical Data Coordinator (CDC) serves as CRF Health?s champion to the world?s largest pharmaceutical and biotech companies in providing clean and accurate data for clinical trials. A CDC is the gatekeeper for this data from study start to finish and is core2/21/2015 Plymouth Meeting, PA Save This Job
Job Code: 14-403 Location: Rockville, MD Applicants must meet the following requirements: Ph.D. or M.S. in biostatistics or related field with a minimum of 7 years experience in the pharmaceutical, biotechnology, CRO industry or related clinical trials environment Experienced1/26/2015 Rockville, MD 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 32/25/2015 Rockville, MD Save This Job
Job Location: San Francisco, CA Description: Responsible for management statistical programming activities and study related projects while also developing and implementing SAS programs to efficiently produce analyses. Exercise judgment within generally defined practices and3/4/2015 San Francisco, CA Save This Job
The Project Manager is responsible for delivering the highest quality ePRO software and service with on-time delivery. The Project Manager will interface with clients as well as the project team. Position Responsibilities: Project Management Facilitate gathering requirements1/25/2015 Boston, MA Save This Job
Position Summary: The Manager of Educational Services is responsible for managing the daily efforts of the Educational Services team, mapping out strategic direction, and for the delivery of role-based curriculum of instructor-led, web-based, and eLearning courses that meet our1/25/2015 Boston, MA Save This Job
Position Summary Reporting to the Chief Scientific Officer, this person is responsible for planning, managing, and completing with the Project Team, all regulatory projects consistent with company goals. The successful candidate will be accountable for timely planning,3/25/2015 Lexington, MA Save This Job