Senior Biostatistician

Highly Competitive Salary
  1. Permanent
  2. Statistics
  3. United States
Boston, Massachusetts
Posting date: 10 Apr 2019
SS.JC.22652_1554910965

ProClinical, in support of our client, are seeking an individual to fill the role of Senior Biostatistician, based in Boston, MA. The successful candidate will be responsible for the statistical activities for multiple clinical studies, participating in protocol development and executions, ensuring compliance with SOPs to produce quality and timely statistical deliverables.

Responsibilities

  • 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 study objectives and 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.
  • Oversee CROs for outsourced statistical activities and QC key results generated by CROs.

Skills And Qualifications

  • MS in biostatistics or related field and 3+ years of relevant clinical trial experience, or PhD with some relevant experience.
  • Knowledge of statistical methods for clinical trials.
  • Proficient in statistical programming (SAS required, R preferred).
  • Strong written, verbal, and interpersonal communication skills.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Junis Citozi at (+1) 9293881650 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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