Clinical SAS Programmer

Please share the resumes to careers@starkassociatesllc.com or

Contact: +1 848-219-9146

Title: Clinical SAS Programmer

Location: Canton, MA

Duration: Long Term contract

How you will contribute:

performing data manipulation, analysis, and reporting of clinical trial data, both safety, and efficacy (ISS/ISE), utilizing SAS programming;

generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs);

production and QC / validation programming;

generating complex ad-hoc reports utilizing raw data;

applying a strong understanding/experience of Efficacy analysis;

communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries;

performing lead duties when called upon;

serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;

being adaptable and flexible when priorities change

What you offer:

Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.

5 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry.

2+ years of study lead experience, preferably juggling multiple projects simultaneously

Strong SAS data manipulation, analysis and reporting skills.

Solid experience implementing the latest CDISC SDTM / ADaM standards.

Strong QC / validation skills.

Good ad-hoc reporting skills.

Proficiency in the Efficacy analysis.

Familiarity with drug development life cycle and experience with the manipulation, analysis, and reporting of clinical trials’ data.

Submissions experience utilizing define.xml and other submission documents.

Experience supporting Oncology studies a plus.

Excellent analytical & troubleshooting skills.

Ability to provide quality output and deliverables, in adherence with challenging timelines.

Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.