Clinical Medical Manager
この求人にエントリーする
求人No. 166728
募集要項
業務内容 |
◆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. |
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語学力 |
要 ・Must have good communication skills and proficiency in both Japanese and English languages. |
年収 |
700万~1500万 |
給与 |
年俸制 賞与 年3回 ※前職を考慮して決定 |
雇用形態 |
正社員 |
勤務地 |
東京都 |
通勤交通費 |
全額支給 |
休日 |
年間休日122日 ■完全週休2日制(土・日) ■祝日 ■年末年始 ■慶弔休暇、育児休業、介護休業 ■積立休暇制度 ■年次有給休暇(初年度12日 最高20日) |
福利厚生 |
各種社会保険完備 ■昇給年1回(4月) ■賞与年3回(3月、6月、12月) ■社会保険完備 ■通勤手当(全額支給)、時間外手当、住宅手当、営業手当、外勤日当、その他各種手当有 ■財形貯蓄 ■企業年金 ■退職金 ■慶弔見舞金制度 ■研修制度 ■借上社宅制度 ■クラブ活動、保養所 ほか |
企業情報
事業内容 |
医療用医薬品、医療機器の開発、輸入・製造、販売 |
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業種分類 |
メディカル/医薬品メーカー |
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