Clinical Data Programmer & CDISC Expert

Fortrea

United States

À distance

USD 90 000 - 120 000

Plein temps

Il y a 20 heures
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Résumé du poste

Fortrea is seeking a clinical data programming professional in the United States to support development and implementation of solutions for Medidata RAVE, Oracle Inform, CRF design, and data capture activities. The role includes creating datasets, CRF annotations, CDISC mapping specifications, and transforming external data into SAS datasets or Excel files for data review.

You will maintain study databases, generate regular and ad hoc reports, and collaborate with study teams to ensure data

Qualifications

  • University/college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • Fluent in English, both written and verbal.

Responsabilités

  • Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities.
  • Develop and maintain programs for creation of datasets as per specifications.
  • Create CRF annotations and Mapping specifications as per CDISC/Sponsor datasets.
  • Develop programs to import external data and transform to SAS Dataset or Excel files for data review and reconciliation.
  • Maintain study databases for assigned projects.
  • Perform programming for reports/listings using SAS/Spotfire.

Connaissances

SAS programming
EDC systems
Data management

Formation

Bachelor's degree in life sciences/IT

Outils

Cognos
Business Objects XI

Description du poste

Fortrea is seeking a clinical data programming professional in the United States to support development and implementation of solutions for Medidata RAVE, Oracle Inform, CRF design, and data capture activities. The role includes creating datasets, CRF annotations, CDISC mapping specifications, and transforming external data into SAS datasets or Excel files for data review.

You will maintain study databases, generate regular and ad hoc reports, and collaborate with study teams to ensure data

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