Senior Statistical Programmer

Cytel; À distance; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading clinical development firm is seeking a Senior Statistical Programmer to support and lead Phase I-IV clinical trials. You will apply advanced SAS programming skills and proficiency in CDISC standards to analyze clinical trial data. This fully remote position requires at least 8 years of experience in SAS programming within the pharmaceutical industry, along with strong data manipulation and validation skills. Enjoy competitive compensation, an excellent benefits package, and opportunities for professional growth.

Prestations

Competitive compensation

Excellent benefits package

Annual bonus incentive

Work-life balance

Qualifications

• At least 8 years of SAS programming experience in the pharmaceutical industry.
• Strong QC and validation skills.
• Solid ADaM and complex TFL skills.
• Proficiency in efficacy analysis.

Responsabilités

• Perform data manipulation and analysis of clinical trial data.
• Generate and validate analysis datasets and complex tables.
• Lead assigned clinical studies under principal programmer’s oversight.
• Communicate with cross-functional teams for project specifications.

Connaissances

SAS programming

Clinical trial data analysis

CDISC standards (SDTM & ADaM)

Data manipulation

Validation programming

QC skills

Efficacy analysis

Ad-hoc reporting

Formation

Bachelor’s degree in Statistics, Computer Science, Mathematics

Description du poste

At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development.

Position is home-based.

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

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.

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.

How you will contribute :

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
• Generating and validating analysis datasets / analysis files, and complex tables, listings, and figures ( TLFs)
• Production and QC / validation programming
• Generating complex ad-hoc reports utilizing raw data and analysis datasets
• Applying 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 for assigned clinical study under principle programmers oversight
• 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
• Generating and validating Non-CDISC transformation datasets and analysis datasets
• Proficient knowledge with SDTM / ADaM and TLF’s. General expertise with Figures
• Individuals should be able to start programs from scratch and have the ability to handle complicated domains and outputs related to the protocol and SAP.
• They must demonstrate a good understanding of the endpoints and data collection, with the ability to read and write specifications related to the respective implementation guides.
• R & complex macro writing are a plus

What you offer :

• Bachelor’s degree in one of the following fieldsStatistics, Computer Science, Mathematics, etc.
• At least 8years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industrywith a bachelor’s degree or equivalent. At least 6years of related experience with a master’s degree or above.
• Study lead experience, preferably juggling multiple projects simultaneously.
• Strong SAS data manipulation, analysis and reporting skills.
• Strong QC / validation skills.
• Good ad-hoc reporting skills.
• Solid ADaM and complex TFL skills.
• Proficiency in efficacy analysis and survival 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
• 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.

Why Cytel?

• Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry.
• In addition to a competitive compensation, we offer an excellent benefit’s package, annual bonus incentive, promote work-life balance, and the opportunity to grow with us!
• Work with respected experts and thought leaders in the fields of biostatistics and statistical programming.