Responsibilities and Requirements :
- Experience working in various disease areas.
- They also must have specific expertise in SDTM programming, have submissions experience, and MUST possess strong skill in graphing.
- They need to be comfortable working as a strong independent contributor who is attentive and speaks up throughout the project work.
- Minimum of years programming experience in the pharmaceutical / biotech industries.
- Experience working in various disease therapeutic areas is required.
- Must have strong SDTM programming skills, ability to create SDTM specifications from scratch and be comfortable with creating ADaM datasets.
- Experience creating source and validation programs using SAS software for SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies / products.
- Regulatory submissions experience.
- Rare disease TA experience is highly preferred.
- The ideal candidate must be able to communicate effectively within a multi-disciplinary project team to assess priorities and complete assigned tasks on time.
- Proficient of SAS programming in a regulated clinical research environment.
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JobPosting","title":"Data Engineer II","datePosted":"2024-04-15T00:00:00","validThrough":null,"description":"Data Engineer II (Multiple Openings), Project Management Institute, Inc. Data Engineer II (Multiple Openings), Project Management Institute, Inc. The position requires a minimum of a Bachelor...
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