Skip to main content

This job has expired

Sr Medidata RAVE Programmer

Employer
Labcorp
Location
Gaithersburg, Maryland, United States;King of Prussia, Pennsylvania, United States;Philadelphia, Pennsylvania, United States;Princeton, New Jersey, United States;Austin, Texas, United States;Toronto, Ontario, Canada;Mississuaga, Ontario, Canada;London, Un
Salary
Competitive
Start date
9 Oct 2019
Closing date
8 Nov 2019

View more

Job Details

Sr Medidata RAVE Programmer

permanent, salaried

Location: Gaithersburg, MD or the UK



RESPONSIBILITIES

Configure 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 (eCRF's) 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 eCRF's 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 description
Experience:
client description
Locations:
Gaithersburg, Maryland, United States;
King of Prussia, Pennsylvania, United States;
Philadelphia, Pennsylvania, United States;
Princeton, New Jersey, United States;
Austin, Texas, United States;
Toronto, Ontario, Canada;
Mississuaga, Ontario, Canada;
London, United Kingdom;
Edinburgh, United Kingdom;
Leeds, United Kingdom;
Slough, United Kingdom;
York, United Kingdom

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert