Clinical Medical Manager

必要に応じて KOL、独立専門家協会、患者支援団体との交流に基づいて医学的/科学的専門知識とアドバイスを提供

仕事内容

The position
・The CMM will facilitate execution of clinical trials related to New Therapy Areas including CKD (Chronic Kidney Disease), CVD (Cardiovascular Disease), Liver Disease, inflammation and Alzheimer’s disease (AD), by providing medical/scientific expertise and advice based on interactions with KOLs, independent professional associations and patient advocacy associations as necessary. The role will report to the Clinical Medical Manager Lead.
・Other role tasks are as follows but is not limited to:

・Identify and map KOLs (Key Opinion Leaders), investigators and research centres within the relevant therapy areas, work closely with clinical operations teams in CDC (Clinical Development Center), region, IO-SO and HQ during feasibility and allocation process, and engage with relevant patient advocacy groups and investigate areas of mutual interest and potential collaboration.
・Collect medical insights that may be of value to Novo Nordisk and cascade these as relevant to region as well as across teams within local affiliate/CDC, optimizing the feasibility process for the clinical trial conduct. The role will also identify and regularly engage with clinical experts in relevant TAs to obtain guidance relevant to clinical trial execution and ensure site staff at main site and referral centres are properly trained.
・Act as subject matter expert within relevant TAs, provide leadership in the scientific community within New Therapy Areas (TA) conducting advisory boards, scientific meetings, guidelines, publications and engaging with local associations for HCPs (healthcare Professionals) on relevant topics, as well as aid in the process on Investigator Sponsored studies by contributing to evaluation of proposals and ensuring follow up after approval in close collaboration with local Medical Affairs team, lead process of mapping of clinical care pathways for new TAs, and help with ad hoc requests by providing scientific and medical responses to requests in a timely manner.
・Contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations, performing ad hoc and planned visits, supporting attendance at investigator meetings, ensuring KOL inclusion in clinical trials, and engaging key investigators to convey trial results, as well as to scientific retention and recruitment (SRR) activities at local level.
・Provide timely guidance and internal training by supporting training creation and delivering training to clinical staff, as well as CMR, commercial and MAPA cross functional teams.

応募条件

【必須事項】

・MD (Medical Doctor) or Ph.D. in healthcare with strong clinical and preferably research background, alternatively Pharmacist or Master of Science with strong, relevant background.
・Must have a minimum of 3 years of clinical or pharmaceutical industry experience, with solid experience with human healthcare research either from university or pharmaceutical industry.
・Expert in therapeutic area of relevance, preferably with authorship in peer-reviewed journals. Experience as clinical trial investigator or sub-investigator is preferred.
・Knowledge on the specificities and nuances of the local healthcare infrastructure, as well as of pharmaceutical drug development
・Must have good communication skills and proficiency in both Japanese and English languages.

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

学歴

大学卒以上

雇用形態

正社員

試用期間

6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　　950万円～　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）最終面接