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.
We are experiencing exponential growth on a global scale and expanding our PBS division and hiring Senior Biostatisticians to lead or help drive one or more clinical studies, across a variety of therapeutic areas. You will report to the Associate Director, Biostatistics.
How you will contribute:
Serve as a study biostatistician for multiple clinical studies
Contribute to clinical protocol development, including authoring of the section on statistical methods and reviewing/editing of other sections by applying statistical principles
Author statistical analysis plans for studies and/or ISS/ISEs, and author/edit shells for tables, figures and listings
Review CRF designs to ensure data collection meet the study objectives and the requirements of statistical analyses
Provide statistical input to data monitoring committee (DMC) charters, project management plans, and other study-level documents
Work with statistical programmers or CROs to generate tables, figures and listings
Support ongoing safety review and DMC review of the clinical development program/study teams
Perform ad hoc and exploratory statistical analyses as needed
Contribute to clinical study reports, including authoring of statistical sections, interpretation of the study results, and QC of the results in the reports.
Support regulatory submissions as needed
Support the preparation of publications, including manuscripts, posters and oral presentations
Provide oversight of CROs for outsourced statistical activities and QC key results generated by CROs
What you offer:
MS in biostatistics or equivalent with at least 3 years of relevant clinical trial experience or PhD in biostatistics or equivalent with some relevant clinical trial experience. For this particular role the MS degree and more junior level experience is most appropriate.
Knowledge of statistical methods for clinical trials
Proficient in statistical programming (SAS is required, and R is a plus)
Good communication skills and ability to work with cross-functional study teams
Ability to multi-task in an extremely fast-paced environment with changing priorities
Ability to solve analytical/technical problems
Positive, outgoing and collaborative attitude
- 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.