Programmer

Overview

Programmer role supporting clinical data management, EDC systems programming and SAS programming for clinical studies.

What you'll do

• 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, including proactive prevention strategies.
• 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 any regular or ad-hoc reports/listings as needed by the Study/Sponsor teams using available tools/SAS/Spotfire.
• Perform database design, EDC/SAS edit programming, listings, and ad-hoc/scheduled reports using SAS/Cognos/Business Objects – XI, R and other tools for data cleaning and reporting.
• Complete assigned work utilizing EDC tools or SAS or other proprietary software according to Fortrea SOPs, Work Instructions, and project-specific guidelines in accordance with Good Clinical Practices (GCP).
• Maintain knowledge and awareness of latest developments in CDISC standards and statistical programming.
• Perform all work with knowledge of regulations pertaining to computerized systems to ensure compliance and interact with project team members in related disciplines.
• Provide regular status updates on the tasks assigned to Line Manager.
• Perform all other duties as needed or assigned.

What you'll need

• 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.
• 3-5 years of relevant work experience to include data management and database support: EDC systems programming or SAS programming.
• Good problem-solving skills and a proactive approach.
• Good oral and written communication skills.
• Ability to work in a team environment and under minimal supervision.
• Ability to prioritize work and self-motivation.
• Appropriate time management skills and the ability to work to tight deadlines while maintaining the highest standards of quality work.
• A cooperative and team-oriented approach.

Nice to have

• Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations.

Details

• Work environment: office environment.