Eli Lilly and Company
<研究開発・メディカルアフェアーズ統括本部>Statistical Analys
Eli Lilly and Company, Indiana, Pennsylvania, us, 15705
研究開発・メディカルアフェアーズ統括本部
Statistical Analyst/ Statistician, Senior Statistician, Principal Statistician /Kobe HQ・Tokyo OfficeAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.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 and statistical summary tables/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 assistance from a statistical analyst point of view.主な職責/Primary responsibilitiesStatistical Analysis Results DeliveryOperate in collaboration with global counterparts to prepare CRT packages appropriately meeting regulatory requirements.Understand selecting statistical methods for data analysis, then prepare programming 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 innovations towards a more efficient working model.Use Communication SkillsetsCollaborate with team members and/or global counterparts to deliver statistical results on time.Coordinate workers dedicated to preparing statistical datasets and outputs.Present topics related to own responsibilities, such as new tools, methodologies, regulatory requirements, etc.Respond to regulatory queries and interact with regulators.Reach out to external parties to shape the environment.Therapeutic Area KnowledgeUnderstand disease states and related medical assessments for preparing appropriate definitions and/or specifications that fulfill statistical analysis objectives.Regulatory CompliancePerform 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 TeamworkIntroduce 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.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.orRich 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.就業場所 神戸本社東京支社従事すべき業務の変更の範囲：当社業務全般就業場所の変更の範囲：将来のキャリアの一環として、神戸本社・東京支社・西神工場・海外オフィスでの勤務をする場合もありうる。Business title:
Statistician, Senior Statistician, Principal Statistician - GSS-J(CS)処遇【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】年一回 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時内で勤務。（ただし、一斉休憩を除く）1日の必要最低労働時間：4時間（半日休暇時は2時間）一斉休憩：12時～13時【在宅勤務制度】有【受動喫煙対策】あり就業場所全面禁煙【休日休暇】完全週休2日制（土・日曜日）、祝日、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日に付与される。Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly
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Statistical Analyst/ Statistician, Senior Statistician, Principal Statistician /Kobe HQ・Tokyo OfficeAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.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 and statistical summary tables/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 assistance from a statistical analyst point of view.主な職責/Primary responsibilitiesStatistical Analysis Results DeliveryOperate in collaboration with global counterparts to prepare CRT packages appropriately meeting regulatory requirements.Understand selecting statistical methods for data analysis, then prepare programming 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 innovations towards a more efficient working model.Use Communication SkillsetsCollaborate with team members and/or global counterparts to deliver statistical results on time.Coordinate workers dedicated to preparing statistical datasets and outputs.Present topics related to own responsibilities, such as new tools, methodologies, regulatory requirements, etc.Respond to regulatory queries and interact with regulators.Reach out to external parties to shape the environment.Therapeutic Area KnowledgeUnderstand disease states and related medical assessments for preparing appropriate definitions and/or specifications that fulfill statistical analysis objectives.Regulatory CompliancePerform 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 TeamworkIntroduce 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.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.orRich 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.就業場所 神戸本社東京支社従事すべき業務の変更の範囲：当社業務全般就業場所の変更の範囲：将来のキャリアの一環として、神戸本社・東京支社・西神工場・海外オフィスでの勤務をする場合もありうる。Business title:
Statistician, Senior Statistician, Principal Statistician - GSS-J(CS)処遇【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】年一回 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時内で勤務。（ただし、一斉休憩を除く）1日の必要最低労働時間：4時間（半日休暇時は2時間）一斉休憩：12時～13時【在宅勤務制度】有【受動喫煙対策】あり就業場所全面禁煙【休日休暇】完全週休2日制（土・日曜日）、祝日、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日に付与される。Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly
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