Clinical Programmer/Sr. Clinical Programmer
The Position
We are seeking a clinical programmer or sr. clinical programmer to join our growing biometrics team to support clinical studies across Arrowhead’s expanding portfolio. This is an exciting opportunity for a clinical programmer with experience in the pharmaceutical industry or at a CRO. They will contribute to the data management, clinical, and statistics team, performing a variety of programming activities.
Key Duties and Responsibilities:
- Work with data managers to develop data review plans to ensure data cleanliness
- Implement SAS-based edit checks to implement data cleaning to ensure data of the highest quality
- Code programs to help reconcile inbound vendor data transfers against clinical database records
- Deliver programming results for ad-hoc analysis requests by statistics
- Develop programs for use by the safety monitoring department to ensure safety surveillance and signal detection
- Review outputs and data transfers provided by CROs for accuracy and consistency with specifications and CDISC Standard
- Assist with vendor oversight to ensure quality deliverables
- Participate in study team meetings and support data-cleaning activities
- Assist in efforts to identify, develop, and implement departmental standards, applications, processes, and training
Requirements:
- Bachelor’s degree in biostatistics/statistics/public health or similar field
- Basic understanding of clinical trials
- Working knowledge of SAS, including complex data manipulation and basic analysis procedures
- Excellent verbal and written communication skills
- At least 1.5 years experience in clinical programming under the pharmaceuticals/biotech clinical development or CROs for the senior position.
- Familiarity with CDISC standards, including CDASH and SDTM
Preferred:
- Familiarity with multiple external data sources including central labs and other electronic data sources
- Familiarity with RAVE
- Exposure to Spotfire or other data visualization platforms.