Contract Spy Remote (United Kingdom)
Jan 23, 2020Duration not stated
Cytel is shaping the future of drug development. As the world 's largest independent clinical biostatistics research and development organization, we help leading pharmaceutical, biotech and medical device companies improve clinical success rates via optimal study design, effective data management, accurate statistical analysis and software. With operations across North America, Europe, and India, we are always on the lookout for passionate and talented people who share our mission of ensuring the clinical development of safe and effective medicines. We are experiencing exponential growth on a global scale and hiring Contract Statistical Programmers to join our FSP division. You will apply your strong proficiency in CDISC standards (SDTM & ADaM) and advanced SAS programming skills, to support analysis of clinical trial data for submission to Health Technology Assessment (HTA) agencies in Europe and across the world. You will report to the Director, Statistical Programming. Position is home-based in Europe, however ideally located in the UK, Switzerland, France or Barcelona. How you will contribute: performing data manipulation, analysis and reporting of clinical trial data, utilizing SAS programming; generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs); generating and updating SAS macros for general use across projects production and QC / validation programming; generating complex ad-hoc reports utilizing raw data; applying strong understanding/experience of Efficacy analysis; communicating with 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 What you offer: Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc. Highly experienced in SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry. Study lead experience is a plus Strong SAS data manipulation, analysis and reporting skills. Strong and independent ability to understand and adapt existing code of varying complexity to new data and subsets 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. Experience supporting Oncology studies a plus. Excellent analytical & troubleshooting skills with proactive communication to anticipate and prevent issues. 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. 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. Cytel does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Cytel’s human resources department to obtain prior written authorization before referring any candidates to Cytel. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Cytel. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Cytel. Cytel shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies.