Senior Statistical Programmer

TN France; France; À distance; EUR 60 000 - 100 000; Plein temps

Résumé du poste

An innovative firm is seeking a Senior Statistical Programmer to join its dynamic team. This fully remote position offers the chance to leverage advanced SAS programming skills and expertise in CDISC standards to support clinical trials across various therapeutic areas. With a focus on collaboration and scientific rigor, you will play a crucial role in data manipulation, analysis, and reporting, ensuring high-quality outputs that meet challenging deadlines. Join a company that values intellectual curiosity and fosters professional growth while working alongside respected experts in the field.

Prestations

Competitive Compensation

Annual Bonuses

Excellent Benefits

Work-Life Balance

Opportunities for Growth

Qualifications

• 8+ years of SAS programming experience in clinical trials.
• Strong knowledge of CDISC standards and statistical reporting.

Responsabilités

• Perform data manipulation and reporting of clinical trial data using SAS.
• Generate and validate analysis datasets and complex tables.

Connaissances

SAS Programming

CDISC Standards (SDTM & ADaM)

Data Manipulation

Efficacy Analysis

Statistical Reporting

Analytical Skills

Formation

Bachelor's Degree in Statistics

Master's Degree in Statistics

Outils

SAS

R

Description du poste

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At Cytel, we work hard to create successful careers with significant professional growth for our employees, which in turn contributes to Cytel's success. Cytel is a place where talent, experience, and integrity come together to advance clinical development.

Position is home-based.

We are experiencing exponential growth on a global scale and are hiring Senior Statistical Programmers to join our FSP division. You will apply your expertise in CDISC standards (SDTM & ADaM) and advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials across various therapeutic areas.

Our values

• We believe in applying scientific rigor to unlock the full potential of data.
• We nurture intellectual curiosity and encourage approaching new challenges with enthusiasm and a desire for discovery.
• We believe in collaboration and value diverse perspectives, leveraging a variety of talents to create possibilities.
• We prize innovation and seek intelligent solutions using leading-edge technology.

As a Senior Statistical Programmer, you will utilize your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead clinical trials. This role can be performed fully remotely.

How you will contribute:

• Perform data manipulation, analysis, and reporting of clinical trial data, including safety and efficacy data, using SAS programming.
• Generate and validate analysis datasets/analysis files, along with complex tables, listings, and figures (TLFs).
• Produce and QC/validate programming outputs.
• Create complex ad-hoc reports from raw data and analysis datasets.
• Apply strong understanding and experience in efficacy analysis.
• Communicate with internal cross-functional teams and clients regarding project specifications, status, issues, or inquiries.
• Lead assigned clinical studies under the supervision of principal programmers.
• Be a team player, willing to go the extra mile to meet results and deadlines.
• Be adaptable and flexible to changing priorities.
• Generate and validate Non-CDISC transformation datasets and analysis datasets.
• Have proficient knowledge of SDTM/ADaM and TLFs; general expertise with figures.
• Start programs from scratch and handle complex domains and outputs related to protocols and SAPs.
• Understand endpoints and data collection, with the ability to read and write specifications aligned with implementation guides.
• Knowledge of R and macro writing is a plus.

What you offer:

• Bachelor’s degree in Statistics, Computer Science, Mathematics, or related fields.
• At least 8 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry for a bachelor’s degree, or at least 6 years with a master’s degree or higher.
• Experience leading studies, preferably managing multiple projects simultaneously.
• Strong SAS data manipulation, analysis, and reporting skills.
• Solid skills in ADaM and complex TLFs.
• Proficiency in efficacy and survival analysis.
• Familiarity with the drug development lifecycle and experience in manipulating, analyzing, and reporting clinical trial data.
• Experience with submissions, including define.xml and other documentation.
• Excellent analytical and troubleshooting skills.
• Ability to produce quality outputs and meet challenging deadlines.
• Ability to work effectively in a globally dispersed team environment with cross-cultural partners.

Why Cytel?

• Our collaborative environment encourages innovation and rewards results. We pride ourselves on one of the lowest turnover rates in the industry.
• We offer competitive compensation, excellent benefits, annual bonuses, promote work-life balance, and opportunities for growth.
• Work with respected experts and thought leaders in biostatistics and statistical programming.