Sr Medidata RAVE Programmer

Other jobs >> General




Recruiter Covance

Location Gaithersburg, Maryland (US)

Salary Competitive

Posted 17 Oct 2019

Closes 14 Nov 2019


Discipline Clinical, Data Management, Medical, Programming

Result Type Jobs

Position Type Permanent

Hours Full Time

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Job Overview:Sr Medidata RAVE Programmerpermanent, salariedLocation: Gaithersburg, MD or the UKRESPONSIBILITIESConfigure and build User and Site Administration modules to include site set up and assignment of roles, permissions and eLearning requirements.

Implementation of industry standards; CDISC-SDTM/CDASH for a Standard Global Library set-up in Medidata RAVE.

Programming of an external data handling of a clinical study data.

Implementing Clinical Dictionaries; such as Thesaurus Management System (TMS), MedDRA and WHO dictionaries.

Configure and build EDC standards in support of clinical studies including, but not limited to, Global Library, Edit Checks, CRF modules and Standard/Custom Reports.

Configure EDC technical support module to facilitate study timelines and deliverables.

Setting up a Global Library Volume in Medidata RAVE DB.

Setting up studies (eCRFs) using Medidata Rave application and using Oracle Clinical global library as a reference during the entire study build.

Creating Projects, Drafts items such as Forms / Fields, Folders, Matrices, Dictionaries, Unit Dictionaries, and other study related items in RAVE as per the eCRFs and study protocol.

Uploading the CRF Guidelines/attachments thru FTP server to the RAVE DB.

Generating reports like RAVE Dictionary Search tool; RAVE Object Search Tool that can be used a reference during study build using Cognos BI

Functions as an EDC Subject Matter Expert (SME) providing guidance and best practice recommendations to Data Management, operations teams and other stakeholders.

Validates specification to development through leading team review, co-programmer review, and User Acceptance Testing.

Setting up the Targeted Source Data Verification (TSDV) configuration of the clinical trial database.

Programming of the custom Business Objects (BO4) reports on the ad-hoc basis for the data validation of the clinical database.

Maintains all required study documentation.

Support development and review of SOPs, and Work Guidelines to promote consistency.

Identify additional opportunities for standardization and departmental efficiency.Education/Qualifications:client descriptionExperience:client description

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