Vacancy expired!
We are Kelly Science and Clinical, the second largest scientific staffing firm in the U.S. serving 90% of Fortune 100 companies. We have partnered with one of the executive branch agencies in the Southwestern United States whose mission is to promote health and wellness, improve health outcomes, and assure safety net services for all people in the State. Overview: The Organization consists of (8) divisions and provides a statewide system of Health Promotion and Community Health Improvement, Chronic Disease Prevention, Infectious Disease Prevention, Injury Prevention, and other Public Health Services. Seeking experienced SAS Programmer supporting clinical trial execution in a Clinical/Medical Laboratory Practice. Hands-on experience with SAS Programming, and with R Programming knowledge, Data Visualization, linking data sets together, and automating SAS programming. Details:
- Position Title: Epidemiologist/SAS Programmer
- Location: Remote
- Position Type: Contract
- Length of Contract: 6 months with potential for extension
- Hourly Rate: $60-$70 per hour
- Excellent Benefits Available through Kelly Services
- Lead/Review SDTM specs, acrf, datasets, Defines, Reviewer's Guide for regulatory, CDISC compliance and SAP.
- Utilize SAS to generate and validate CDISC SDTM, ADaM compliant datasets and TLFs based on SAP. Utilize SAS to generate any ADHOC related analysis for various needs (internal, publications, etc.).
- Oversight to ensure quality and timely deliverable. Collaborate with cross functional teams on ongoing basis representing statistical programming on Study Management Teams
- Collaborate with cross functional teams on ongoing basis representing statistical programming on Study Management Teams
- Review eCRFs, DMP and other Data Management documents. Review Statistical Analysis Plan.
- Legally authorized to work in the job posting Country.
- Bachelor's degree in statistics, mathematics, computer science, management information systems, or related field of study is required; MS in statistics or biostatistics is desirable.
- The successful candidate for this position will have a proven track record of SDTM/ADAM, TLFs programming supporting clinical trial execution and regulatory submissions.
- Strong knowledge with FDA and CDISC/SDTM requirements for compliant datasets, programs, and validation processes is a must have.
- Experience with Data Visualization and linking Data Sets together.
- Heavily involved in designing, developing & validating CDISC SDTM specifications and datasets.
- Experience with producing outputs submitted to the FDA and other regulatory agencies.
Vacancy expired!