Clinical Trials Specialist
4 weeks ago
Transforming Clinical Development with Fortrea
At Fortrea, we are committed to revolutionizing the drug and device development process. As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development solutions.
Key Responsibilities
- Develop and maintain SAS programs to create SDTM datasets, ADaM datasets, generate tables, listings, and figures, and perform QC of SDTM, ADaMs, and tables, listings, and figures.
- Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs, and Reviewers Guides to support SDTMs and ADaMs.
- Collaborate with senior programming staff to develop specifications for SDTMs and ADaM datasets.
- Review SAPs and TFL shells from a programming perspective and provide feedback to senior programming staff.
- Support QA and client audits with senior programming staff.
About Fortrea
Fortrea is a dynamic and innovative company that is passionate about scientific rigor and excellence. We offer a collaborative workspace where personal growth is nurtured, and our team members have the opportunity to make a meaningful global impact.
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