SAS Clinical Applications Developer

job summary:
Job Description :

Supporting safety and efficacy analysis in Immunology projects

Interpreting information from aCRF, SDTM data, SAP and SPP to develop ADaM specifications and ADaM datasets to support CSRs

Supporting ISS/ISE ADaM programming and submissions

Develop and review TLF outputs

Experience/Skills :

6 to 8+ yrs of SAS programming experience, preferably in UNIX environment, supporting clinical trials data analysis. Enterprise Guide experience is a plus.

Solid CDISC Standards knowledge, 8+ years of ADaM and TLF programming experience supporting safety and efficacy analysis. Immunology TA experience is preferable but not required.

Well experienced in converting information from aCRF, SDTM data, SAP and SPP into ADaM specifications and review TLF outputs from vendors.

Experienced in supporting ISS, ISE ADaM programming and submissions.

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.

Back-up contact for programming of tables, listings, and graphs for a specified compound project. Responsible for the validation and quality assurance of any output produced for specified projects and contributing to al project management such that timelines are met. Back-up participant on Clinical Project teams representing clinical programming efforts for that clinical team. Prefer candidate with clinical experience. SAS program experience required.

 
location: Telecommute
job type: Contract
salary: $60 - 68 per hour
work hours: 9am to 5pm
education: Bachelors

responsibilities:

Job Description :

• Supporting safety and efficacy analysis in Immunology projects
• Interpreting information from aCRF, SDTM data, SAP and SPP to develop ADaM specifications and ADaM datasets to support CSRs
• Supporting ISS/ISE ADaM programming and submissions
• Develop and review TLF outputs

qualifications:
6 to 8+ yrs of SAS programming experience, preferably in UNIX environment, supporting clinical trials data analysis. Enterprise Guide experience is a plus.

Solid CDISC Standards knowledge, 8+ years of ADaM and TLF programming experience supporting safety and efficacy analysis. Immunology TA experience is preferable but not required.

Well experienced in converting information from aCRF, SDTM data, SAP and SPP into ADaM specifications and review TLF outputs from vendors.

Experienced in supporting ISS, ISE ADaM programming and submissions.

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.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad Digital, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on randstadusa.com.


Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad Digital offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.