Jobs in Rockville
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Job Title
Employer Type
Found 540 jobs
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Data Manager/Protocol Monitor (International)
Coordinate site selection and site initiation activities for international sites Determine data collection requirements for new protocols Design sour
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Clinical Data Manager
Work in a team environment to design, develop and manage clinical trial data systems, supporting materials, and processes, including the EMMES propri
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In-House Clinical Research Associate
Possesses detailed knowledge of the study protocol and its associated activities and timelines Participates in the preparation and/or review of draft
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Talent Director
Work in collaboration with Emmes Project Leaders and Functional Group Managers to manage the internal deployment of talent in accordance with contrac
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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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Administrative Coordinator
Provide day-to-day coordination between operational staff Aid in the design, development consolidation and distribution of reports, manuals, presenta
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Programmer Analyst-DICOM Experience
B.S. in Computer Science or related field with at least 2 years of relevant experience Good object oriented programming skills Working knowledge of t
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Software Architect
Maintains broad knowledge of emerging and well-established technologies and frameworks on the market, design patterns, best practices, and standards
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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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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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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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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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Biostatistician-PhD
Collaborates with clinical investigators to determine study design Writes sections of protocols that require statistical input Reviews protocols and
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CIRB Document Control Specialist
Provide support to CIRB Coordinators for the management of multiple IRBs; Provide updates to Monthly Progress Report; Post documents to website as re
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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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Programmer Analyst
B.S. in Computer Science or related field with at least 2 years of relevant experience Good object oriented programming skills Working experience of
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Clinical Research Specialist
Participates in study team meetings and Operations Center staff meetings ยท Interacts with study site staff to obtain site specific regulatory docum
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ABA Instructor
The Autism Program serves students from ages 5-21 with Autism Spectrum Disorder. Applied Behavior Analysis, systematic teaching, and data based pro...
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