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data analysis sas cdisc sdtm adam๐ Description
- Lead and/or support programming efforts to deliver SAS analysis components.
- Work under the Programming team leader to ensure quality and timelines.
- Client-facing role with a high-trust environment and independent work.
- Deliver scalable, robust programming solutions for CVRM studies.
๐ฏ Requirements
- Strong SAS programming experience in pharma/CRO.
- Hands-on CVRM study programming experience.
- Experience generating SDTM, ADaM, and TLFs.
- Good CDISC standards and trial process knowledge.
- Ability to work independently and manage multiple priorities.
- Strong communication and stakeholder management skills.
๐ Benefits
- Direct sponsor engagement and additional career opportunities.
- Security and career growth within a global CRO.
- Collaborative client-facing environment.
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