日本イーライリリー株式会社 日本イーライリリー株式会社

【研究開発本部バイオメトリクス】
Project Statistician (担当/担当課長/専門課長)
職務内容 【職務概要/Overall Job Purpose】
Provide strong statistical leadership in the process of drug development.
The Project statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues. The Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.


【主な職責/Primary responsibilities】
Statistical Trial Design and Analysis
● Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.
● Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created.
● Collaborate with data management in the planning and implementation of data quality assurance plans.
● Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
● Participate in peer-review work products from other statistical colleagues.

Communication of Results and Inferences
● Collaborate with team members to write reports and communicate results.
● Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
● Respond to regulatory queries and to interact with regulators.

Therapeutic Area Knowledge
● Understand disease states in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

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. 
応募要件 【必須経験(Required Experience (mandatory for hiring)】
◆ M.S. or Ph.D. in statistics or biostatistics.
or
◆ Rich experiences in healthcare field as a statistician with science background such as mathematics or epidemiology.

◆ Ph.D. more preferable


【望ましい経験/Desirable Experience】
◆ Experiences of collaboration with team outside of Japan (preferred: overseas living experience)


【必須応募資格/Essential skills and license (mandatory for hiring)】
◆ Statistical and methodological knowledge in clinical development, epidemiology or related field.
◆ Regulatory knowledge of clinical trial methodology and statistics.
◆ Ability to build relationships with individuals and teams.
◆ Strong English and Japanese communication and presentation skills


【望ましい資格/Desirable skills and license】
◆ Proficient in the SAS programming language 
待遇  【給与】当社規定により優遇します
【諸手当】住宅手当、通勤交通費など
【昇給】有り
【賞与】年1回(個人業績結果、及び会社業績結果に基づく業績変動賞与を翌年3月に支給する)
【勤務時間】8:45〜17:30
【時間外手当】”担当職”のみ支給
【清算制フレックス勤務】適応あり。フレキシブルタイム:5時〜22時(昼休憩を除く)、昼食休憩:12時〜13時
【休日休暇】完全週休2日制(土・日曜日)、祝日、クリスマス、年末年始・夏期
*年間休日125日、年次有給休暇、慶弔等
【保険】雇用・労災・健康・厚生年金保険
【福利厚生】住宅援助制度、借上社宅制度、リリーグループ補償制度(医療費・歯科医療費補助制度等)
【定年制】有(60歳)
【継続雇用制度】有(65歳まで)
【有給休暇】
 年途中で入社した社員に対する年次有給休暇は、次の入社月の区分に従い入社の翌月1日に付与さる。入社日にかかわらず、その年の12月31日をもって、勤続年数が1年経過したものとみなし、翌年1月1日に翌年度の年次有給休暇が付与される。


入社月  1〜6月  7月  8月  9月 10月 11月 12月
付与日数  10日  5日  4日  3日  2日  1日  0日

【試用期間】 正社員 6か月間(試用期間中での賃金の違いはございません) 
勤務地  神戸本社 


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