Real World Evidence Manager

リアルワールドエビデンス（RWE）の分野で戦略的な取り組みやプログラムを推進

仕事内容

・As the Real-World Evidence Manager, you will be accountable for managing the real-world evidence planning, execution, and analyses within the assigned therapeutic or functional area with partners and vendors to improve patient care and support the business needs in alignment with the Japan evidence generation plan. You will utilize the Novo Nordisk real-world data platform, partnership platforms and analytic tools while developing and maintaining stakeholder relationships to communicate the RWE strategy ＆ data and to ensure the optimal utilization of RWE.
The role responsibilities are as follows but are not limited to:

・Drive innovation in RWE data by implementing new analytic methods, platforms, and technologies to answer research and business questions. Conduct analyses using internal and external real-world data to generate unique disease insights and epidemiological information to improve patient care and support business needs.
・Prepare study outlines and study protocols, informed consent, and amendments. Provide input to study and project related documents. Ensure the availability of other study related documents. Create plans for the operational management of real-world studies, including Gantt Chart and ensure timely deliverables.
・Implement project management tools and coordinate timely delivery of relevant components of documents. Ensure audit and inspection readiness and handling protocol deviations (if applicable) to ensure high compliance.
・Acts as a partner for Japan stakeholders within Medical, Clinical, Regulatory, PMS, Safety, Market Access, and commercial teams, as well as a liaison to therapeutically aligned Global counterparts (Epidemiology, Data Science, Real-World Evidence, etc.) in assigned therapeutic or function area.
・Maintain relationships with external stakeholders such as investigators, co-investigators, KOL, medical experts, health authorities, agencies and vendors and manage communication effectively with the Study Group and Contract Research Organization (CRO) including study progress information.

応募条件

【必須事項】

・PhD or master’s degree in fields related to Epidemiology, Biostatistics, Health Services Research and Health Economics.
・Must have experience writing high-quality protocols and other study documents and conducting statistical analysis in Real World observational studies. Pharmaceutical industry experience is preferred (Experience in Market access and Health Economic and Outcomes Research will be a plus).
・Must have more than 2 years of recent work experience in non-interventional research, including longitudinal studies with RWD assets (e.g., claims, electronic health records, and/or surveys) in a pharmaceutical company, contract research organization, health care provider or academic institution.
・Strong business acumen, teamwork, cross functional collaboration skills, fluent level in English and Japanese language skills at least at business level are essential.
・Ability to negotiate, reach an agreement and secure progress on deliverables through flexibility, creativity, and compromise.
・ Excellent process and project management skills including the ability to manage a significant volume of projects with good triage and judgment skills is preferred.

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

学歴

大学院修士以上

雇用形態

正社員

試用期間

3ヶ月

勤務地

東京

転勤の有無

転勤なし

受動喫煙防止措置

屋内禁煙

勤務時間

フレックスタイム制
フルフレックス（コアタイムなし）

勤務開始日

応相談

休日休暇

年間休日数：129
土日祝
年間有給休暇：入社半年経過時点10日　10日 ～ 20日
法定休暇：年次有給休暇、産前産後休暇、介護休暇
その他休暇：ボランティア休暇、リフレッシュ休暇など

年収・給与

年収　　600万円～1200万円　経験により応相談

諸手当

通勤手当（全額支給）、時間外手当、住宅手当、その他各種手当有
MRの場合上記に加え、営業手当、外勤日当を支給

昇給

年1回

賞与

年2回

採用人数

若干名

待遇・福利厚生

通勤手当：有
確定拠出年金制度

各種制度

健康保険：有
雇用保険：有
労災保険：有
厚生年金：有

選考プロセス

１）書類選考
２）一次面接
３）二次面接
４）最終面接