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Clinical Spotfire/SAS Programmer
Job Description
Our client is seeking a highly skilled Clinical Spotfire/SAS Programmer to join their team remotely. This role offers an exciting opportunity to leverage advanced programming expertise in SAS, Spotfire, R, Python, and SQL within a dynamic clinical research environment. The successful candidate will support the development of CDISC-compliant datasets, build interactive dashboards, and contribute to regulatory submissions, ensuring data quality and integrity throughout all phases of clinical trials. With a focus on rare disease research and clinical pharmacology, this position provides a unique platform for professional growth, exposure to cutting-edge data management techniques, and meaningful contributions to impactful health outcomes.
Responsibilities:
Requirements / Qualification:
Responsibilities:
- Develop and validate SAS programs to generate data review, cleaning, and reconciliation listings.
- Program listings, tables, profiles, figures, and standard datasets per the best practices, standard processes, and specifications as needed. Generate supporting validation and quality check documentation.
- Execute existing SAS programs and macros. Perform debugging and error resolutions. Identify and implement improvements.
- Perform user administration in the EDC using the templates and best practices.
- Develop and apply SAS macros/SQL to increase programming efficiency.
- Perform data mappings between different data sources and standard output using industry standard best practices, annotated CRFs.
- Perform data quality checks along with supporting documentation.
- Develop data visualization packages per the requirements and standard specifications as needed.
- Analyze, process, execute data reconciliation and data integration requirements and develop programs as applicable.
- Provide input on and facilitate specifications development on complex reports/listings.
- Accountable for programming deliverables for the assigned studies, tasks, and/or programming projects.
- Â Assist in resolving data issues with the data providers.
- Perform quality checks and assessment on internally and externally developed programs and data packages.
- Provide support to routine programming, validation, and documentation activities.
- Collaborate with data managers and study team members.
- Assist in statistical programming activities as needed.
- Perform quality control checks on programmed data and reports to meet regulatory standards and internal guidelines. Identify and address data quality and consistency issues.
- Maintain detailed documentation of programming activities, code development, and validation processes.
Requirements / Qualification:
- Experience developing clinical visual analytics with Spotfire
- Data wrangling using Spotfire
- Proven experience in Pharma/Biotech/SAS Programming - Bachelor’s degree or higher in the scientific, biological, statistical or computer science field or related discipline.
- M.S. in Stats/Math/Epidemiology degree preferred.
- Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills
- Must be proficient in programming skills (e.g. SAS Certified).
- Academic/industry projects demonstrating solid use of programming techniques and/or programming platforms is a plus.
- Must be a fast learner and be able to adapt to changing situations.
- Must operate with High Integrity and Trust.
- Personal Accountability: Will stand up and be counted; doesn’t shirk personal responsibility; is comfortable working alone on tough assignments
- General knowledge of industry standards and best practices such as CDISC/CDASH, SDTM, data standardization.