Principal Sr. SAS Programmer - Efficacy CDISC SAS Rock Star- (Remote, USA) job
Principal   Sr. SAS Programmer - Efficacy CDISC SAS Rock Star- (Remote, USA) job
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Principal / Sr. SAS Programmer - Efficacy/CDISC/SAS Rock Star- (Remote, USA) Job

Employer Name: Cytel, Inc. SpiderID: 7091092
Location: Raleigh, North Carolina Date Posted: 11/13/2017
Wage: Category: Biotech
Job Code: SASPrg
Number Of Openings: 20

Job Description:
Cytel’s FSP division is growing and hiring home-based Sr. Statistical Programmers with a successful track record supporting clinical trials, to join our team supporting one of the world’s leading Biotech companies.

Leveraging your strong technical aptitude and SAS programming skills, along with exceptional multi-tasking abilities and can-do-attitude, you will provide statistical programming support for Phase I-IV clinical trials across varying therapeutic areas. You will work primarily on complex ad-hoc requests, and QC output, heavily utilizing raw data and your experience in Efficacy analysis.

You will make a difference by…

• performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming;
• applying your CDISC know-how and proficiency in both SDTM and ADaM, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s);
• QCing (using raw data) and validating the work of outsourced teams requiring strong output programming;
• generating complex ad-hoc reports utilizing raw data;
• applying your strong understanding/experience with Efficacy analysis;
• performing lead duties when called upon;
• serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
• being adaptable and flexible when priorities change

This is a REMOTE position with the option to be office-based at our office in King of Prussia, PA or Waltham, MA.

Job Requirements:
What we need from you…

• Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
• Minimum 8 years of SAS programming experience in the Pharmaceutical & Biotech industry.
• 2+ years of study lead experience, preferably juggling multiple projects simultaneously.
• Strong experience in QCing and validating work of other programmers, preferably outsourced work.
• Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience
• Ability to implement the latest CDISC SDTM / ADaM standards.
• Strong ad-hoc reporting and the use of raw data.
• Solid experience in Efficacy analysis.
• Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
• Ability to work in a development environment that utilizes minimal utilities and standard macros.
• Submissions experience utilizing define.xml and other submission documents.
• 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.

Cytel offers a competitive salary, with an annual bonus incentive, excellent benefit’s package and the opportunity to GROW with us!

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required: 8
Education Required: Bachelors
Overnight Travel: None
Vacation Time: 3 weeks / year

Job Benefits:
Health/Dental Benefits, Retirement Benefits, Paid Holidays, Vacations, and Sick Leave, Life and/or Disability Insurance, Offers Sponsorship for U.S. Visa, Other Benefits

Company Profile:
Cytel is shaping the future of drug development. As the world's largest independent clinical biostatistics research and development organization, Cytel helps leading pharmaceutical, biotech and medical device companies improve clinical success rates via optimal study design, effective data management, and accurate statistical analysis. Cytel provides both software solutions for the design and analysis of clinical trials, including industry standards East®, StatXact® and LogXact®, as well as data focused clinical research services. With operations across North America, Europe, and India, Cytel employs 900 professionals, with strong talent in biostatistics, programming, and data management. For more information on Cytel, please visit:

Contact Information:
Contact Name: Diana Skubiak Company Type: Employer
Company: Cytel, Inc. Phone: 407.890.1012
Street: Fax:
City: Cambridge
State: Massachusetts
Zip: 02139

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