🔍 About Fortrea
Fortrea Holdings Inc. is a globally recognized Contract Research Organization (CRO), headquartered in Durham, North Carolina, and operates across 90+ countries. It provides advanced clinical trial solutions to major pharmaceutical, biotechnology, and medical device companies.
🚀 Job Overview – Programmer Analyst Role
As a Programmer Analyst at Fortrea, you’ll work on multiple concurrent clinical research projects. This role demands strong skills in SAS programming, data visualization, clinical data analysis, and report generation using tools such as Medidata RAVE, Tableau, or Spotfire.
You will play a key part in transforming raw clinical data into regulatory-compliant formats for submission and reporting while learning from senior team members or mentoring others when needed.
✅ Key Responsibilities
- Perform independent SAS programming and data manipulation tasks for clinical studies.
- Develop/validate CRF annotations, SDTM datasets, and Define XML/Reviewers Guide for regulatory submission.
- Create and maintain visual dashboards with Spotfire/Tableau.
- Manage study databases and import/export data for reconciliation or analysis.
- Ensure timely and quality delivery of datasets and reports in line with CDISC/Client standards.
- Coordinate across teams, prioritize tasks, and address technical and compliance issues.
- Train and mentor junior programmers in tools like SAS, RAVE, and Oracle Inform.
- Work independently on multiple projects and contribute to process improvements.
✅ Required Skills & Tools
- Programming: SAS, R, Python, SQL
- Tools: Medidata RAVE, Oracle Inform, Tableau, Spotfire
- Standards: CDISC, SDTM, ADaM
- Reporting: Cognos, Business Objects XI
- Compliance: GCP, 21 CFR Part 11
📈 Why Join Fortrea?
- Work on cutting-edge clinical trials with a global leader.
- Exposure to cross-functional clinical data operations.
- Career advancement with structured learning and mentoring.
- Collaborative and fast-paced work environment.
📝 How to Apply
Click the link below and apply before. Don’t miss the chance to grow your career in global clinical research programming.
