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The ideal candidate will have varied experience in electronic data collection technologies, such as Veeva EDC, Medidata Rave, and Oracle InForm, etc., as well as an in-depth knowledge of programming tools as a representative of data and analytics processes across functional initiatives.
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Proficient in cross collaboration with other functions such as Biostatistics, Statistical Programming, Pharmacovigilance and Clinical Operations. Experience with Medidata Rave preferred. Works closely with database builders during programming of EDC databases, edit checks and reports.
$149,125 - $156,360 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Expertise with EDC systems, such as Medidata Rave, InForm, Medrio. Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom programming.
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Proficiency with Medidata Rave EDC, Clinical Data Repositories and Visualization software. The Clinical Data Manager will be responsible for daily data management tasks for all phases of clinical trials including CRO/vendor oversight and support other functional areas such as clinical operations, statistical programming, and biostatistics.
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A thorough understanding of the drug development process from pre-IND through registration and post-registration and a broad understanding of functional areas of drug development, including (preclinical, regulatory, pharmacology, translational medicine, pharmacovigilance, data sciences (data management, biostatistics, programming), and clinical operations is require.
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Experience with real world evidence databases (e.g., Medrio, InForm, RedCap, OpenClinica, RAVE) a plus. Solid hands-on knowledge of at least one programming language (e.g., Python, SAS, R MATLAB, Sharp, Visual Basic, SQL required.
$107,064 - $167,911 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with clinical data management systems, proficiency in EDC/RDC (e.g. RAVE, Inform, Oracle Clinical), experience in basic SAS / SQL programming, and an understanding of CDISC, SDTM and other industry standards, experience with reporting tools like J-review is a plus.
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SAS, Programmer, statistics, CDISC, SDTM, ADaM, CRO, clinical research, pharmaceutical, biotechnology, clinical data, data management, EDC, Electronic Data Capture, Medidata, Rave, Oracle, Inform, datasets, TLF, tables, listings, figures, programming, benefits, medical, dental, vision, 401k, Remote.
$130,000 - $145,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Overall responsibilities will include supporting clinical data management activities from study start-up through study closure in support of trial objectives and corporate goals. Experience and understanding of ICH, GCP and CDASH/CDISC are required.
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Experience with Medidata Rave. Provide programming support for study team members from the study start up to the end. Minimum of 3 years hands-on SAS programming experience in a pharmaceutical environment.
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Experience in technologies such as Medidata modules (RAVE, Coder, RTSM, eCOA), Veeva eTMF, eClinical Solutions Elluminate, SAS LSAF. Overseeing or acting as intermediate between Data Management, Statistical Programming and external data provider regarding external data specifications, data, and technical issues.
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Good knowledge of statistical programming languages (e.g., SAS, R, Python, etc. Desirable technical expertise (e.g., Windows NT and UNIX operating systems) and familiarity with common software products and technologies used in conjunction with SAS, familiarity with Rave and/or Veeva.
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Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE. Serve as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE. Must have background in Pharmaceutical / Biotechnological companies.
RemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave. Provide technical support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modules.
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