|We are seeking a Biostatistician to join our high growth global Clinical Research Services business unit based in Paris. Candidates will also be considered for our offices based in Geneva or Barcelona. For experienced candidates remote or part time remote positions across Europe can also be considered.
This is a high impact role providing statistical input into Phase I - IV clinical trial development, performing the analysis of clinical trial data, and providing statistical input into the reporting of clinical trial results.
Your responsibilities will include:
Providing statistical input into protocol and case report form (CRF) development in all therapeutic areas (e.g., trial design, sample size estimation, randomization, statistical methods for protocols, edit checks for clinical trial data); communicating with clients regarding study protocol or statistical analysis issues; and writing detailed statistical analysis plans including specifications for analysis files, consistency checks, tables, and figures.
Additionally, you will analyze clinical trial data producing accurate results representing the outcome of the trial, validate statistical output, accurately interpret and clearly communicate statistical results and concepts to non-statisticians. With the medical writer, you will co-author final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix for the final report. You also will provide statistical output as required for manuscripts and ensures that the results are accurately interpreted in the publications.
In this role you will provide input into statistical standard operating procedures (SOPs) and general standardization efforts (e.g., statistical methodology standards, standard data presentations) and participate in interactions with regulatory agencies, as required. You will be expected to collaborate effectively with members (internal and external) of clinical trial implementation teams and with Biometrics colleagues, and keep abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetings.
Qualifications and Experience
You will have a PhD degree in Statistics or Biostatistics or related field with some applied statistics training relevant to the clinical trials or health research environment, and one (1) year of relevant work experience or a Master’s degree in Statistics or Biostatistics or a related health science field and at least 5 years of statistical experience in the clinical trials or health research environment.
Additionally, we require excellent written and oral communication skills including grammatical/technical writing skills, and familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials.
Compensation & Benefits
We offer competitive salary-based package, bonus, comprehensive medical health insurance and pension.
Who We Are
The clinical development of drugs and devices is crucial for human welfare. Our mission is to improve success rates in this endeavor.We do this by improving the design and implementation of clinical trials through the innovative application of statistical science, operations research, and information technology.
What We Do
We provide unrivalled biostatistics and operations research knowledge to our customers. Our knowledge is available in the form of both software and services. This knowledge, supported by our trial implementation capabilities, is what makes us different. We are leaders in the design and implementation of adaptive clinical trials.
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.
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