Clinical SAS Programmer

Job Description

Primary Responsibilities:

• Manage data management projects, focusing on technical delivery and data-related tasks.
• Utilize technical expertise in SAS, SQL, R, or other programming languages.
• Familiarity with data reporting tools like JReview, SAS JMP, Tableau, etc.
• Coordinate with statisticians and programmer/analysts.
• Collaborate with clinical research and development, clinical operations, and CROs to develop study documents.
• Ensure data management tasks align with study timelines and requirements.
• Conduct ongoing data review and collaborate with CROs to identify and correct errors or discrepancies.
• Communicate site data concerns/issues to the clinical operations team and CROs for resolution.
• Ensure delivery of a quality locked database for analysis at the study's close.
• Recommend technical and process solutions to improve project work efficiency.
• Establish programming standards and comply with regulatory requirements.
• Develop standard macros and tools in SAS for data analysis.

Skills Required:

• Experience with EDC systems like Medidata Rave.
• Familiarity with MedDRA and WHODD coding.
• Knowledge of CDISC SDTM and CDASH standards.
• Strong understanding of clinical trial operations.
• Proficiency in data programming and visualization tools (JReview, Tableau, etc.).
• Excellent communication, organizational, problem-solving, conflict resolution, project leadership, and team-building skills.

Preferred Skills:

• Experience in Oncology, Neurology, and Nephrology.
• Knowledge of global trials.
• Previous experience in smaller bio-oncology companies.
• Familiarity with Immuno-Oncology.

Education:

• Bachelor's degree or equivalent in math, science, or a health-related field.