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Clinical Data Standards Consultant

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Clinical Data Standards Consultant

Pharmaceuticals

United Kingdom

Description

Data Standards consultant - Home based role (UK)

We require a Data Standards consultant to develop project and company standard metadata structures and provide guidance and support.

Role

Develop project and company standard metadata structures
Provide support and knowledge to project teams on the company and industry standards (eCRF creation through to SDTM domains)
Work in therapeutic area focus groups to align and improve processes
Define and release company metadata structures within the MDR system
Define and maintain EDC global library elements, including eCRFs, fields, data dictionaries, and procedure specifications
 Reviewing Controlled Terminology under RAVE/MDR/SDTM systems
 

Experience

You will be experienced within clinical standards within the Pharma or CRO/Vendor industry
You will have an in-depth comprehension of CDISC standards
Experience with Data mapping and eCRF creation through to SDTM domain
Good written and oral communications skills in the English language.
Excellent communication skills and able to work with cross-border teams
Experience with RAVE is a plus but not essential

 

This will be a fixed-term role for 2 year

 

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Job Details

  • Job Type:

    Permanent
  • Salary:

    Negotiable
  • Job published:

    22 days ago
  • Reference:

    BH8570/P