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採用企業 | 日本イーライリリー株式会社 |
勤務地 | 東京都 23区 |
雇用形態 | 正社員 |
給与 | 600万円 ~ 経験考慮の上、応相談 |
【求人No NJB2231126】
職務内容
Provide strong statistical leadership in the process of drug development.
The statistical analyst provides strong leadership in the process of drug development by preparing CDISC complied databases statistical summary table/figures in accordance with a schedule. During the development of protocol designs data analysis plans and regulatory interactions it is expected to collaborate with relevant study team members and provide assists from statistical analyst point of view.
主な職責/Primary responsibilities
Statistical Analysis Results Delivery
・ Operate in collaboration with global counterparts to prepare CRT packages appropriately meet with regulatory requirements.
・ Understand selecting statistical methods for data analysis then prepare programing codes for delivering analysis datasets and outputs accordingly.
・ Collaborate with data management in the planning and implementation of data quality assurance plans.
・ Maintain currency with respect to standards dictionaries computational tools for statistical methodology and regulatory requirements.
・ Obtain project management skillset to coordinate delivering database and/or statistical outputs.
・ Participate in peer review work products from other statistical colleagues.
・ Seek for any innovations towards more efficient working model realized.
Use Communication Skillsets
・ Collaborate with team members and/or global counterparts to deliver statistical results on time.
・ Coordinate workers dedicated to preparing statistical datasets and outputs.
・ Present any topics related to own responsibilities such as new tools methodologies regulatory requirements etc.
・ Respond to regulatory queries and to interact with regulators.
・ Reach out external parties to make environmental shaping happen.
Therapeutic Area Knowledge
・ Understand disease states and related medical assessments for preparing appropriate definitions and/or specifications that fulfills statistical analysis objectives.
Regulatory Compliance
・ Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate Medical local and departmental policies procedures processes and training.
Statistical leadership and Teamwork
・ Introduce and apply innovative methodology and tools to solve critical problems.
・ Merge scientific thinking and business knowledge to identify issues evaluate options and implement solutions.
・ Lead projects independently and work effectively across functions. Apply technical expertise to influence business decisions.
職務経験 | 無し |
キャリアレベル | 中途経験者レベル |
英語レベル | ビジネス会話レベル |
日本語レベル | ネイティブ |
最終学歴 | 大学卒: 学士号 |
現在のビザ | 日本での就労許可が必要です |
以下についてはStatistician Senior Statistician Principal Statisticianに対する要件で御座います。
必須経験/スキル・資格
どちらかを満たす方
・ M.S. in statistics biostatistics or computer science but not limited to. Any relevant certifications would be acceptable.
or
・ Rich experiences in healthcare field as a computational statistician with science background such as biology or epidemiology.
・ Statistical/methodological knowledge and computational skill in clinical development epidemiology or related field.
・ Regulatory knowledge of clinical trial methodology and statistics.
・ Ability to build relationships with individuals and teams.
・ Good communication and presentation skills in both English and Japanese
雇用形態 | 正社員 |
給与 | 600万円 ~ 経験考慮の上、応相談 |
勤務時間 | 08:45 ~ 17:30 |
休日・休暇 | 【有給休暇】初年度 10日 2か月目から 【休日】完全週休二日制 年末年始 完全週休2日制(土・日曜日)、祝日、クリスマス、年… |
業種 | 医薬品 |
会社の種類 | 外資系企業 |