Jobs in Rockville
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Found 453 jobs
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Production Specialist
Planet Depos is a global court reporting company providing best-in-class court reporting, videography, videoconferencing and interpretation service...
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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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Biostatistician-MS
Collaborates with clinical investigators to determine study design Writes sections of protocols that require statistical input Reviews protocols and
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Employee Relations Manager
Recommend policy and procedure to align with overall employee relations strategy Develop employee relations programs which strengthen overall employe
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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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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 ยท Interacts with study site staff to obtain site specific regulatory docum
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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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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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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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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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CRA Manager
Coordinates all monitoring aspects in the execution and support of clinical trial activities Supervises and ensures CRA team members are compliant wi
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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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Energetic Customer Service Associate
Job Summary/Company: Do you feel comfortable dealing with people and carrying out administrative duties with accuracy and speed? If so, this role i...
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