At 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. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

＜職務内容＞

Purpose:
The Clinical Project Statistician develops or assists in the development of protocol designs, clinical plans, and data
analysis plans in collaboration with physicians, clinical research scientists, and other research colleagues. The
Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting
database and for analyzing data for clinical studies.

Primary Responsibilities:
This job description is intended to provide a general overview of the job requirements at
the time it was prepared. The job requirements of any position may change over time and may include additional
responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job
responsibilities and any related duties that may be required for the position.

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon
current business needs.

Statistical Trial Design and Analysis
▪ Provide input on study protocol, design studies and write protocols for the conduct of each study.
▪ Be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of
the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is
created.
▪ Collaborate with data sciences in the planning and implementation of data quality assurance plans.
▪ Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied
methods, and to be competent in justifying methods selected.
▪ Perform peer-review of work products from other statistical colleagues.
▪ Influence team members regarding appropriate research methods

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 interact with regulators.

Therapeutic Area Knowledge
▪ Understand disease states, competitive landscapes, and regulatory environment 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.

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.

•従事すべき業務の変更の範囲 ：「当社業務全般」

•就業場所：日本、神戸本社　東京支社および在宅勤務の場所を含む

•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＞

＜ 必須経験/スキル・資格 ＞

Minimum Qualification Requirements:
▪ M.S., Ph.D., or equivalent experience
▪ Statistics, Biostatistics, or equivalent of field study.

▪ 2025年日本イーライリリー医薬品開発職入社内定者

-弊社では社員のウェルビーイングと生産性の観点から、自宅最寄り駅から勤務地までの通勤距離が90㎞以内かつ公共

交通機関の所要時間*が90分以内の範囲を、通勤可能上限としています。

それよりも遠方にお住まいの場合は、通勤可能な範囲にご転居いただくことを原則としております（借上社宅の貸与あ

り）。車両通勤を認める場合においても、上記を適用します。

＜ ＞

Other Information/Additional Preferences:
▪ Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUGs, etc
▪ Interpersonal communication skills for effective customer consultation
▪ Teamwork and leadership skills
▪ Technical expertise and application with working knowledge of experimental design and statistical analysis
▪ Self-management skills with a focus on results for timely and accurate completion of competing deliverables
▪ Resource management skills
▪ Creativity and innovation
▪ Demonstrated problem solving ability and critical thinking
▪ Business process expertise associated with critical activities (e.g., regulatory submissions)

＜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】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支給する。

　支給時期は、営業職は9月および翌年3月に支給、非営業職は翌年3月に支給。

【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　全面禁煙

【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翌月1日に付与される。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  　 5  　4　　3  　 2  　　 1  　　 0

【試用期間】 6か月間　　試用期間中での賃金の違いはありません。

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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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.

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