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Job opening ID73 Posting titleClinical Data Manager Roles and responsibilitiesAs the Clinical Data Manager at Penumbra, you will ensure the integrity of clinical data, supporting multiple clinical teams and studies. Specifically, you will: ?Ensure that data quality and integrity3/26/2016 Alameda, 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 the3/28/2016 Cambridge, MA 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?3/20/2016 Boston, MA Save This Job
Job Description The Clinical Project Manager provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities? regulations/guidelines, and applicable SOPs.3/20/2016 Boston, MA Save This Job
Location: South San Francisco, CADepartment: Research and DevelopmentType: Full TimeMin. Experience: Experienced About Second Genome: Understanding the conversation taking place between our bodies and the millions of bacteria residing within the gut is key to unlocking profound3/27/2016 South San Francisco, CA 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 to4/13/2016 Cambridge, MA Save This Job
The Clinical Program Manager (CPM) is responsible for the independent coordination and management of one or more multi-center studies within a program. The CPM is expected to oversee vendors and contract research organizations, ensuring that Calithera?s clinical activities are3/27/2016 South San Francisco, CA Save This Job
Clinical Development Scope of Responsibilities The Clinical Program Manager is assigned to lead and manage multiple small clinical trials or a large phase 3 study. Oversee all operational aspects including budgets, timelines, resources, vendor selection and management as well as3/1/2016 San Francisco, CA Save This Job
Reporting to the Chief Medical Officer, the Senior Clinical Trial Manager will be responsible for the day-to-day management of ChemoCentryx clinical trials, including management of contract CROs conducting company sponsored clinical trials. Specific Responsibilities Work with3/28/2016 Mountain View, CA Save This Job
Position Summary: Primary responsibility of the Product Manager is to coordinate and manage the development, launch and maintenance of Halfpenny?s existing and new software solutions for clinical data exchange. Duties and Responsibilities: Acquire and maintain a working knowledge3/22/2016 Blue Bell, PA Save This Job
Department: Clinical Operations Location: Emeryville, CA Position Summary The Clinical Study Manager (CSM) is responsible for the day to day management of a clinical trial(s) in the United States and possibly other countries for the ZX008 program and will manage the study3/20/2016 Emeryville, CA Save This Job
Job Description: Alder is seeking an experienced Clinical Project Manager (CPM) to expand our growing Clinical Operations department. This position will perform a wide variety of activities to support the startup and completion of clinical research studies and may supervise3/19/2016 Bothell, WA Save This Job
Job Description: The Manager, Clinical Data Management will oversee the selection of vendors/CROs (e.g. review RFPs, attend CRO audits); manage or coordinate work performed by the vendor/CRO, including in-house data management specialist(s), in support of data management4/18/2016 Bothell, WA Save This Job
POSITION SUMMARY: Manages the design, administration and on-site monitoring of clinical trials sponsored by Second Sight. Supervises CRAs in in-house and on-site monitoring. Oversees adherence to SOPs, GCP, and FDA regulations. Ensures compliance with clinical protocols, overall2/29/2016 Sylmar, CA Save This Job
Company:Data Sciences International Job Location(s):Minneapolis, MN; New Brighton, MN; St. Paul, MN Start Date:ASAP Employment Term:Regular Employment Type:Full Time Hours per Week:40 Work Hours (i.e. shift):1st Starting Salary Range:Not Provided Required Education:Bachelor's4/19/2016 Minneapolis, MN Save This Job
Clinical Development Scope of Responsibilities The Senior Clinical Data Manager is responsible for overseeing Data Management (DM) operational activities, ensuring compliance with the corporate timeline and scope of work outsourced to the DM service provider (SP) and coordinating3/31/2016 San Francisco, 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 class3/15/2016 Audubon, PA Save This Job
Morrisville, NCFull-time Company Description Liquidia Technologies, founded in 2004, is a privately held biotechnology company located in Research Triangle Park, North Carolina. By leveraging precise fabrication techniques of the semiconductor industry, Liquidia has become the4/4/2016 Morrisville, NC 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 with4/26/2016 Rockville, MD Save This Job
Apply Now Email 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 treat3/27/2016 Rockville, MD Save This Job