Jobs in Rockville
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Job Title
Employer Type
Found 459 jobs
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Supervisor, Operation Compliance (893-679)
This is a key hands-on and supervisory position in the Central Laboratory Operations (CLO) department responsible for several aspects of operations...
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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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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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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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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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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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Programmer Analyst
B.S. in Computer Science or related field with at least 3 years of relevant experience Good object oriented programming skills Working esperience of
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Recruitment Representative
Perform full life-cycle recruitment functions (source, recruit, screen, schedule and coordinate candidate interviews, reference/background check proc
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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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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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CDISC Data Manager
Review protocols for CDISC conformance Develop and review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements Utilize proprieta
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GCP Clinical Junior Auditor
Work closely with the QA Associate and the Quality Management Representative in support of Emmes's corporate Quality Assurance Department Support / l
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Clinical Research QA Specialist
Conduct internal audits to identify non-compliance in adherence to SOPs, regulations and GCPs Work closely with the QA Associate and the QA Manager i
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