As a leader in next generation, data-driven pharmaceutical services, Cytel is shaping the future of drug development. We deliver to the market innovative analytical software for statistical analysis and simulation, best-in-class data science analytics services and high-end impact consulting. Our culture is inclusive, collaborative and results-driven with a shared commitment to quality. With operations across North America, Europe, and India, Cytel hires passionate and talented people who share its mission of ensuring the clinical development of safe and effective medicines.
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, to support or lead one or more Phase I-IV clinical trials, across a variety of therapeutic areas. You will report to the Associate Director, Statistical Programming.
This is a home-based position in Europe, with the option to work from our Geneva, Basel, Paris and Barcelona office locations.
How you will contribute:
performing data manipulation, analysis and reporting of clinical trial data, data pooling and analysis of both safety and efficacy (ISS/ISE), utilizing SAS programming;
generating and validating ADaM datasets/analysis files, and tables, listings, and figures ( TLFs);
production and QC / validation programming as well as overseeing CRO deliverables;
generating ad-hoc report, analyses for publication etc.;
applying strong understanding/experience with Efficacy analysis;
communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries;
performing lead duties at trial level or for other activities 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
What you offer:
Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
5-8 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 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 is desirable.
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.
Proactive and effective communication skills
Meaningful Work, Collaborative Culture, Stimulating Challenges
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 benefits 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.
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.
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