JAC Recruitment ハイクラス転職エージェント

求人・転職情報

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CSLベーリング株式会社

仕事内容
■Position Purpose:
Provide an overview of the responsibilities of the position by providing a summary of the most important aspects and duties of the position.

The Statistical Scientist provides components of statistical contribution to a clinical development program. The Statistician implements statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables. The position will support the Japan clinical/PMS team with statistical expertise, ad hoc analyses and interpretation of requests from PMDA. The Statistical Scientist will collaborate with the global CSL team on the design of global studies including Japan and on stand-alone studies conducted in Japan only. It is expected that the candidate will be experienced with PMDAs requirements regarding CDISC and to communicate these effectively to the global Biostatistics.

■Main Responsibilities and Accountabilities:
List the roles and responsibilities of the position (please limit the number of responsibilities to the primary ten.)
-Support Biostatistics to conduct study data collection, data analysis, reporting, and submission preparation.
-Be accountable for timely completion and quality of the statistical analysis plan.
-Manage outsourcing operations for assigned projects.
-Ensure timeliness and quality of deliverables by CRO, and conduct reviews of CRO deliverables to ensure quality.
-Support Biostatistics and data management related interactions with authorities (especially PMDA), including submissions to PMDA.
-Be responsible for compilation of the CDISC deliverables for the PMDA submissions and ensure its quality per the PMDA requirement.
-Be responsible for result accuracy in study report and regulatory submission documents.
-Manage preparation for the GCP inspections and lead the discussion at the on-site sponsor inspections related to data science areas (biostatistics, data collection and data management)
-Conduct ad hoc statistical analyses.
-Support improvement initiatives and related standards for infrastructure / process / scientific consulting.
求める経験 / スキル
■Position Qualifications and Experience Requirements:
Provide hiring requirements for the specified position, including educational, experiential, and competency requirements necessary for the position.

▷Education
PhD or MS in Biostatistics, Statistics, or related fields.

▷Experience
-At least 5 years of experience in Clinical Development in a Pharmaceutical or Biotechnology setting
-Japan native preferred; Strong interpersonal and communication skills (verbal and written in English and Japanese)
-Ability to collaboratively work and provide leadership in a matrix environment
-Statistical support in facilitating and optimizing clinical development programs, especially for global studies including Japan (sample size in rare diseases)
-Knowledge of CTD and CDISC submission requirements (SDTM and ADaM) for PMDA is highly preferred
-Experience managing CRO preferred
-Basic knowledge of clinical development and processes
-Experience with statistical programming using the SAS software
-Ability for overseas travel (mainly USA) once/twice a year
-Desired: Advanced knowledge and training in applications of statistical methodologies
従業員数
290名 (2020年現在)
勤務地

東京都

想定年収

1,150 万円 ~ 1,800 万円

従業員数
290名 (2020年現在)

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