
Senior Data Specialist
3 days ago
About the Role:
This is an exciting opportunity to work with a highly skilled team in the pharmaceutical industry. As a Senior Data Specialist, you will be responsible for providing high-quality data solutions to support clinical trials and research projects.
Key Responsibilities:
- Develop and implement SAS programs to convert data from EDC systems to protocol-specific SAS datasets.
- Validate edit check programs using standard validation practices and processes.
- Assist in the creation of project programming and validation documentation.
- Develop SAS macro and format libraries.
- Review and approve User Requirement Specifications (URS), Clinical Data Management (CDM) conventions, and related documents.
- Maintain the SAS environment, providing assistance with installation, updates, and maintenance.
Requirements:
- Bachelor's degree in Computer Science or a related field.
- 8+ years of SAS programming experience in the pharmaceutical industry.
- 5+ years of experience working with CDISC, SQL, and Relational Databases.
Skills and Qualifications:
- Strong attention to detail and a meticulous approach to work.
- Excellent communication skills, both verbal and written.
- Strong documentation and organizational skills.
About Us:
We are a dynamic organization committed to delivering high-quality data solutions. We offer a collaborative and supportive work environment, with opportunities for professional growth and development.
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