Clinical Application Specialist III – Statistical SAS Programming
TR/080805
Posted: 29/01/2026
- $65 - $75 per hour
- United States, Remote work
- Contract
Clinical Application Specialist III – Statistical SAS Programming
Hourly Rate: $65-75/hr
Location: 100% Remote
Contract: 1 year - based on performance and business needs
Responsibilities:
Complete assignments from lead programmers on time and with good quality; provide updates to study lead programmer and peer programmers as needed. ADaM programming and validation, TFL programming and validation, additional quality review of statistical programing deliverables; communicate with programming team on issues of various types.
Qualifications:
What hours and days will this person be working?
9am – 5:30pm CST including 30 mins lunch break, Monday to Friday
What are the top 5 skills/requirements this person is required have?
MS in Statistics, Computer Science or a related field with 5+ years of relevant experience. or BS in Statistics, Math, Computer Science or a STEM related field with 8+ years of relevant experience.
What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
What positions/background experience do you feel are successful in this role?
Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Hourly Rate: $65-75/hr
Location: 100% Remote
Contract: 1 year - based on performance and business needs
Responsibilities:
Complete assignments from lead programmers on time and with good quality; provide updates to study lead programmer and peer programmers as needed. ADaM programming and validation, TFL programming and validation, additional quality review of statistical programing deliverables; communicate with programming team on issues of various types.
Qualifications:
- 5+ yrs of experience in Statistical Programming using SAS preferably in UNIX environment, supporting clinical trials data analysis. Enterprise Guide experience is a plus.
- Solid CDISC Standards knowledge, and solid ADaM programming experience including both safety and efficacy analyzes. Oncology TA experience is preferred.
- Experienced in supporting ISS, ISE ADaM programming and submissions is a plus.
- Ability to quickly learn internal macros, processes and interpret Pinnacle 21 results.
- Team player with excellent communication skills and experience working with stat programmers, statisticians and data management personnel.
What hours and days will this person be working?
9am – 5:30pm CST including 30 mins lunch break, Monday to Friday
What are the top 5 skills/requirements this person is required have?
- Dataset and TLF generation and validation for clinical trials using SAS
- CDISC knowledge, familiarity with ADaMIG, ADaM specification experience
- Understand study documents and common safety and efficacy analyses
- Teamwork, effective communication
- Oncology Therapeutic Area experience or knowledge
- Regulatory submission experience or knowledge
MS in Statistics, Computer Science or a related field with 5+ years of relevant experience. or BS in Statistics, Math, Computer Science or a STEM related field with 8+ years of relevant experience.
What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
- SAS certification
- Prefer candidates w/ SAS EG and Unix environment experience.
- SAS Studio experience is a plus as well
What positions/background experience do you feel are successful in this role?
- Pharmaceutical or related industry experience with clinical trials
Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Rachael Jalbuena
Recruitment Consultant
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