Senior Statistical Programmer PBS

Cytel; Caen; À distance; EUR 80 000 - 110 000; Plein temps

Résumé du poste

A leading company in the pharmaceutical sector seeks a Senior Statistical Programmer to leverage advanced SAS skills for clinical trials. This remote role requires extensive experience in data manipulation, Efficacy analysis, and adherence to CDISC standards. The ideal candidate will thrive in a collaborative environment, ensuring high-quality outputs under tight deadlines.

Qualifications

• At least 8 years of SAS programming experience in the Pharmaceutical & Biotech industry.
• Study lead experience, preferably juggling multiple projects simultaneously.

Responsabilités

• Performing data manipulation, analysis, and reporting of clinical trial data.
• Generating and validating SDTM and ADaM datasets/analysis files.
• Communicating with internal cross-functional teams and clients.

Connaissances

SAS programming

data manipulation

Efficacy analysis

QC / validation skills

ad-hoc reporting

Formation

Bachelor’s degree in Statistics

Bachelor’s degree in Computer Science

Bachelor’s degree in Mathematics

Description du poste

Position (CANADA BASED) Overview:

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.

Our values

• We believe in applying scientific rigor to reveal the full promise inherent in data.

• We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.

• We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.

• We prize innovation and seek intelligent solutions using leading-edge technology.

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 strong understanding/experience of Efficacy analysis

• Creating and reviewing submission documents and eCRTs

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

• Being adaptable and flexible when priorities change

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

• Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.

• At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.

• Study lead experience, preferably juggling multiple projects simultaneously preferred.

• 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 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 immunology, respiratory or oncology studies would be 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.

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.