Jobs in Rockville
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Job Title
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Found 572 jobs
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Nutrition Program Aide
The position of Nutrition Program Manager is for the Bauer Park Senior Nutrition Program.
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Data Scientist Intern
Westat is an employee-owned corporation providing research services to agencies of the U.S. Government, as well as businesses, foundations, and sta...
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Regulatory Document Specialist
Performs key TMF system administrator role and duties in accordance with the company guidelines and work instructions (e.g., TMF set-up, quality mana
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Oracle EBS Application Specialist (913-679)
The United States Pharmacopeial Convention has an opening for Oracle EBS Application Specialist in Rockville, MD. Provide expert functional and hig...
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SAS Programmer
Provide statistical programming support for multiple clinical research projects Produce datasets, analyses, tabulations, graphics and listings of cli
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Business Analyst-Clinical Systems Analyst
Manage a project’s software development life cycle for data capture applications (i.e., AdvantageEDC, GlobalTrace, etc.) from requirements gathering
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Biostatistician-PhD or experienced MS
Collaborates with clinical investigators to determine study design Writes sections of protocols that require statistical input Reviews protocols and
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Associate Programmer/Analyst
B.S. in Computer Science or related field Good object oriented programming skills Knowledge of two or more of the following skills: Java, Servlets, J
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Data Manager/Protocol Monitor
Strong data management/computer skills; experience with CRF design, EDC systems, or other web based data collection systems helpful Attention to deta
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Regulatory Affairs Specialist
Participates in the development of regulatory strategies to advance new drugs, biologics, and devices through the clinical trial and licensure proces
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Clinical Research Specialist
Participates in study team meetings and Operations Center staff meetings · Interacts with study site staff to obtain site specific regulatory docum
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Senior Programmer/Analyst
Designs, develops, implements and maintains web-based clinical trials data collection applications in a J2EE environment Has primary responsibility f
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Clinical Research Project Manager
Coordinate the activities and supervise the project study team Liaison with the study sponsors and the collaborating investigators to prepare and ini
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IRB Local Context Coordinator
Responsible for reviewing and processing all submissions from participating institutions for completeness before CIRB review and complete an administ
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Product Manager
Defines requirements for software product based on market research and stakeholder feedback Prioritizes requirements based on business value, return
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Programmer Analyst
B.S. in Computer Science or related field with at least 3 years of relevant experience Good object oriented programming skills Working experience of
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Home-Based Clinical Research Associate/Protocol Monitor
Responsible for writing and distributing time sensitive site visit reports, tracking resolutions of outstanding issues, and ensuring compliance with
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Clinical Protocol Specialist
Possesses detailed knowledge of the protocol and its associated activities and timelines Participates in the preparation and/or review of protocol an
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Clinical Information Specialist/Steering Committee Coordinator
Communicates continuously and effectively with the NCI and Committee membership Plans and coordinates all regularly scheduled and ad-hoc conference c
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