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EDC RAVE Programmer

Employer
Labcorp
Location
Europe
Salary
On application
Start date
6 Sep 2020
Closing date
6 Oct 2020

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Discipline
Data Management / Statistics
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Our Company :

Joining Covance Flexible Solutions (FSPx) will offer a rewarding career, a chance to work in an energetic & team oriented workplace, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Our unique opportunity will allow you to bring your specialized discipline to a core team outsourced to a world class leading global healthcare company. Dedicated to our Client 100% of the time, you will play a key role in the drug development cycle and see a product through to launch with the support of both a dedicated Covance line manager and our client project teams.

 

Your role:

The EDC RAVE Programmer role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor.

    • Communicate effectively with the Project team in order to meet/exceed sponsor requirements. Take action where required in order to meet the timelines and deliverables.
    • Work with the study teams and management advising and informing on the processes that have to be completed to enable the technology to be implemented. Encourage interest and build confidence in the systems.
    • Advise management regularly on the status and any potential risks or issues with on-going projects to ensure resolutions in a timely manner.
    • Configure and build User and Site Administration modules to include site set up and assignment of roles, permissions and eLearning requirements.
    • Configure and build EDC standards in support of clinical studies including, but not limited to, Global Library, Edit Checks, Custom Functions, CRF modules and Standard/Custom Reports.
    • Setting up studies (eCRFs) using Medidata Rave application and using Oracle Clinical global library as a reference during the entire study build.
    • Validates specification to development through leading team review, co-programmer review, and User Acceptance Testing.
    • Maintain all required study documentation.
    • Support development and review of SOPs, and Work Guidelines to promote consistency.
    • Identify additional opportunities for standardization and departmental efficiency.
    • Perform other duties as required by the department
    • Additional preferred experience:
      • Medidata Certified Study Builder.
      • Implementation of industry standards; CDISC-SDTM/CDASH for a Standard Global Library set-up in Medidata RAVE.
      • Setting up Targeted Source Data Verification (TSDV) configuration of the clinical trial database.
      • Setting up Medidata Coder.
      • Custom Function programming.
      • Report programming, preferably Crystal/SQL.

REQUIREMENT:

 

  • Previous or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
  • Experience in a clinical development environment
  • Experience in, or knowledge and understanding of, Medidata Rave, including database build and custom function programming
  • Peferred experience:
    • Implementation of industry standards; CDISC-SDTM/CDASH for a Standard Global Library set-up in Medidata RAVE.

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

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