Global trials for oncology, rare diseases and other complex diseases face unique challenges. Precision partners with our clients to meet them head-on through our extensive footprint across the globe. We succeed by pairing personalized clinical services with translational medicine excellence, making us the first fully integrated clinical research organization created expressly to help advance the promises of precision medicine.
Modern biomarker-informed therapeutic and diagnostic development programs involve a complex operational and data ecosystem. Multiple data streams flow from sites, central labs, and specialty labs.
At Precision, we understand that data isn't enough. Clients need information, or data with context, to make decisions that impact patient health
Position Summary
The SAS Report Programmer, programs metrics, reports and tools for the support of the clinical trial data cleaning process from study start up to post database lock for assigned projects using the SAS software.
Essential functions of the job include but are not limited to:
- Ensures on-time delivery, communicates the status of SAS programming projects to internal teams and study
- Provides collaborative input and guidance to the design of SAS outputs to the client and internal teams
- Programs metrics, reports, tools, patient profiles
- Develops, tests, and validates SAS programs to support client-related and cross-functional projects
- Troubleshoots and resolves SAS program issues
- Develops and maintains SAS programming validation documents
- May provide biostatistics support for client-related projects which may include tables, listings, figures, SDTM, ADaM and various other CDISC deliverables
- May provide data management support for client-related projects from CRF design to post database close and archival
- May participate in conducting demonstrations and trainings
- May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to SAS programming activities
- Provide leadership for cross-functional and organization-wide initiatives, where applicable
- Trains project team members
- Communicates with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
- Present software demonstrations/trainings, department/company training sessions, present at project meetings
- May require some travel
- May perform other duties as assigned
Qualifications
Minimum Required:
- Bachelor's degree or equivalent in local country or equivalent level of experience
- 3+ year of experience in a clinical, scientific or healthcare discipline
- Solid experience in generating reports, listings, Proc SQL, macros, Jreview
Other Required
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
- Able to handle a variety of clinical research tasks
- Excellent organizational and communication skills
- Professional use of the English language; both written and oral
- Experience in utilizing various clinical database management systems
- Experience in a clinical, scientific or healthcare discipline
- Advanced computer skills
Preferred
- Experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), R, SQL
- Oncology and/or Orphan Drug therapeutic experience
- Base SAS, SAS/STAT and SAS/ACCESS software
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. 2020 Precision Medicine Group, LLC
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [Confidential Information].
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