【製薬オンライン】製薬会社・製薬メーカー・製薬企業・医薬品・医療機器等の製薬・医療業界の求人転職サイト

受付時間 平日9時~20時まで 土曜9時~17時まで 03-6278-8721

製薬業界専門の転職・求人サイト 製薬Online.com
最終更新日: 2019年 03月 05日
期間限定!2019年3月31日まで最大10万円の転職お祝い金を進呈!

会社概要

世界各国に拠点があり、製品と開発を拡充しつづける製薬メーカー

設立年
2000年
本社所在地
東京都 
事業内容
医療用医薬品の開発、製造及び販売 

この会社の求人情報

7件中1~7件を表示しています。

新着

求人管理No.008196

外資製薬メーカーにてMSL【呼吸器領域】

科学的・医学的ブランド認知を高め、医療従事者と深い討議を行う

外資製薬メーカーにてMSL【呼吸器領域】

募集要項
呼吸器疾患/アレルギー領域のScientific expertとして顧客の1次対応窓口として関係構築をおこない、メディカル活動を牽引頂きます。呼吸器領域における製品を担当し、新製品の上市前準備、上市後の製品価値の最大化に向け疾患・製品啓発のための活動を行って頂
きます。
・最新の医学・医科学情報をもとにKEEとディスカッションをおこない、
 呼吸器領域におけるUnmet medical needs・インサイトの収集と分析
・呼吸器領域における、エビデンスに基づいた疾患・病態・製品価値に関
 する説明
・上市前製品(未承認薬/承認薬の用法/用量適応外を含む)の質問に対し科学的中立な立場からエビデンスに基づいたリアクティブな情報提供
・科学的に中立な立場で実施するScientific Exchange Meetingの企画
・メディカルが主催するイベントの実施支援(Advisary boardmeeting, medical booth活動など)
・医師主導型研究のコンサルティング
・学術発表/論文作成に関するメディカルコンサルテーション 
募集条件
・製薬企業あるいは大学における研究経験(目安:3年以上)
・呼吸器/アレルギー疾患/自己免疫疾患領域・製品経験
・ビジネスレベルの英語力(目安:TOEIC700点以上) 
勤務地
東京、大阪

求人管理No.013129

【循環器領域】MSLへ転職

外資製薬メーカーに循環器領域におけるMSL活動

【循環器領域】MSLへ転職

募集要項
循環器領域のScientific expertとして顧客の1次対応窓口として関係構築をおこない、メディカル活動を牽引頂きます。
循環器領域における製品を担当し、新製品の上市前準備、
上市後の製品価値の最大化に向け疾患・製品啓発のための活動を行って頂きます。

・最新の医学・医科学情報をもとにKEEとdiscussionを行い、循環器領域におけるUnmet medical needs/インサイトの収集と分析
・循環器領域における、エビデンスに基づいた疾患・病態・製品価値に関する説明
・学術発表:論文作成に関するメディカルコンサルテーション 
募集条件
・循環器領域での経験者
・製薬メーカーにてMSL経験
・ビジネスレベルの英語力(TOEIC:700点以上) 
勤務地
東京、大阪

求人管理No.011876

オンコロジー領域MR

オンコロジー領域のMRをご担当いただきます。

オンコロジー領域MR

募集要項
外資製薬メーカーにてオンコロジー領域のMRをご担当いただきます。 
募集条件
《必須経験》
■基幹病院担当MR経験3年以上

《必須保有資格》
■MR認定資格
■普通運転免許

※英語力:不問 
勤務地
全国各地

求人管理No.013179

Risk Management & Safety Scientists

Safety surveillance representatives lead to execution of pharmacovigilance activity, and communication of Safety Assurance Measure basically during EPPV period.

Risk Management & Safety Scientists

募集要項
Risk Management & Safety Scientists are responsible for setting product safety specifications and for delivery of local Risk Management Plan (RMP), and J-PI (safety parts) to optimize market access from patient safety perspective in Japan.
RMP Team Leads manage setting the project safety strategy in view of ‘Benefit and Risk valance’ of each product by planning the appropriate risk minimization activities and pharmacovigilance plan including regulatory mandatory pharmacovigilance studies collaborated with JPT and Global Strategic Safety Management Team (SSaMT) Leads for JNDA preparation.
Safety surveillance representatives lead to execution of pharmacovigilance activity, and communication of Safety Assurance Measure basically during EPPV period. 
募集条件
■Experience
【Mandatory】
・Bachelor’s or higher Degree in Science or related discipline
・Relevant safety experience or experience elsewhere in Pharmaceutical industry
・Cross-functional project team experience
・Thorough knowledge of the Pharmacovigilance or drug development process
・Written and verbal communication skills
・Scientific knowledge sufficient to understand all aspects of safety issues

【Nice to have】
・Pharmacovigilance activities, Drug development or regulatory affairs experience in outside of Japan
・Working with external bodies, such as co-marketing companies and advisory board members, as a leading person

■Skill-set
【Mandatory】
・Communication/negotiation skill
・Leadership skill
・Problem solution skill
・Logical thinking
・Business English (Speaking level 6 or above)
・Understanding of PMD Act, relevant regulations, GVP/GPSP and guidelines
・Basic knowledge of pharmacoepidemiology and statistical analysis
・Expertise of medical/pharmaceutical science in general 
勤務地
東京・大阪

求人管理No.012658

Assosiate brand manager(乳がん)

乳がん製品におけるブランドマーケティングの求人

Assosiate brand manager(乳がん)

募集要項
ABM for Lynparza Breast cancer
Responsivities are below.
・Drive BC products ( FAS, Lyn BC) success
・Deliver promotion materials with strict time manner
・Create the innovative materials, considering how MRs use them effectively and how MRs can give impacts to costumer
・Contribute to manage promotional events; national meetings, and events which are cosponsored with medical society
・Contribute to create to manage and conduct MR training
・Effective inputs to brand paln , especially from MR point of view
・Help to manager core brand team meeting, which is cross functional team
  ・Monitoring KPIs
  ・Monitoring MRs activities
  ・Analysis from data
  ・Help to facilitate the meeting
・Close communication with sales persons, RMP and DMs to obtain inputs from real world in order to reflect materials
・ Close communication with medical team , especially MA/MSL to get effective medical insight in timely manner and to check if MKT and Medical have same direction according to agreed strategy
・Build strong relationship with top KEEs to create materials and manage events effectively, timely
・Help to create National sales plan every half year
・Keep policy strictly  
募集条件
《Experience》
Mandatory:
Career level: Above D(more than M4 or M3)
・Good business communication skill
・Logical thinking
・Analysis findings
・Presentation skill for structure, ppt design
・Scheduling ; planning and management
・Stakeholder consensus building 

Nice to have:
・Minimum of at least 7+ years experience in pharmaceutical industry
・Pharmacy qualifications to have discussion with external customers
・Basic knowledge about ovarian cancer and our OC related products

《Languages》
Mandatory:
Japanese Fluent
TOEIC more than 500 
勤務地
大阪

求人管理No.013199

外資製薬メーカーのMRの求人

循環器・代謝/消化器領域におけるMR業務

外資製薬メーカーのMRの求人

募集要項
MRとして、製品および患者ニーズのエキスパートとして、専門医を訪問します。主要な顧客との長期的な関係を築き上げ、売り上げに貢献します。 
募集条件
必須:
・MR経験(3年程度以上)
・MR認定資格
・普通自動車免許
・過去10年以内にコンプライアンス、法令等の違反による懲罰歴がないこと
・過去3年以内に道交法違反による自動車運転免許の停止・取り上げの処分を受けていないこと

歓迎:糖尿病領域の経験、新薬上市経験、基幹病院担当経験 
勤務地
応相談

求人管理No.012025

Japan Project Physician

外資製薬メーカーにて臨床開発を主導する医師の募集。

Japan Project Physician

募集要項
Description:
Project Physician (PP) is a medical expert who is accountable/responsible for the medical science expertise to generate clinical development strategy, design clinical development options, and deliver successful clinical development of responsible products in Japan. PP is working closely with Medical Scientist (MS). His/Her accountability/responsibility is mainly project-level, however, he/she is also involved in study-level activities as needed.

1 Project Level
1.1 Design & Interpretation / D&I
1.1.1 Lead D&I activities to generate Japan clinical development strategy with MS and ensure that Japan medical science views are appropriately incorporated in project development strategy
1.1.2 Generate high-quality design options that characterize benefit, risk and value of medicinal products, focusing on reducing uncertainties and providing clear and transparent recommendations for decision and governance bodies.
1.2 Planning
1.2.1 Ensure and champion consistent clinical science aspects and strategies across programs.
1.2.2 Ensure optimal management of high impact project opportunities and risks.
1.2.3 Review study design, regulatory documents consistent with the clinical strategy.
1.2.4 Ensure delivering rationalized hypothesis, evidence based argument, and convincing interpretation in clinical science related documents.
1.2.5 Input scientific information to internal documentation/slides such as IDP/CDP and governance document.
1.3 PMDA interaction
1.3.1 Co-develop clinical science part of regulatory related documents with MS; e.g., PMDA consultation BD, query responses, etc., and ensure the consistency with agreed clinical strategy and medical science aspects are captured properly.
1.4 JNDA
1.4.1 Review CTD and ensure the consistency with agreed clinical strategy and medical science
aspects are captured properly.
1.5 Pharmacovigilance (PV)
1.5.1 Evaluate the safety data, describing industry’s views for patient safety in CTD preparation, and
point out information required for safety narrative and DSUR.
1.6 KEE management
1.6.1 Lead key contacts with external experts and help develop clinic-scientific alliance working with
MS and global CPT.
1.6.2 Act as a key point of contact for clinical science related relationship with external experts.

2 Study Level
2.1 Planning
2.1.1 For Japanese standalone studies including regulatory required post-marketing studies, lead
development of clinical science part of clinical trial documents with MS, e.g., study specification,
clinical study protocol.
2.1.2 For global leading studies including Japan, review the document and ensure that medical
scientific feasibility and ethical integrity in Japan is appropriately incorporated.
2.2 Execution
Act as a study physician of Japan standalone studies as well as support global study physicians of
global leading studies to care for the following tasks:
2.2.1 Provide clinical science support such as eligibility criteria, efficacy and safety data review to
specific studies for risk mitigation.
2.2.2 Ensure the medical/scientific accuracy in following documents:
2.2.2.1 CSPs (incl. Master Informed Consent Form) and CSRs.
2.2.2.2 IND and responses to Regulatory Authority.
2.2.3 Approve following documents as a study physician:
2.2.3.1 Study specification (SS), Clinical Study Protocol (CSP) and Clinical Study Report
(CSR)
2.2.3.2 (if applicable) Japan specific part of Investigator Brochure (IB)
2.2.3.3 Medical contents of Case Report Forms (CRFs).
2.2.4 Lead discussion at Investigators’ meeting.
2.2.5 Lead executing GPRMP for clinical studies.
2.2.6 Provide clinic-scientific leadership to non-interventional study planning and reflect results on
Japan D&I activities.
2.2.7 Provide clinic-scientific leadership and support ESR in Japan.
2.3 Publication
2.3.1 Input to publication strategy and contents/quality of publications

3 Collaboration with Marketing company
3.1 Input scientific and medical perspectives into Japan commercial, pricing and medical strategy for
product value maximization

4 Others
4.1 Compliance to company rules and external regulations
4.1.1 Ensure that own work and all work within TA is performed in accordance with appropriate SHE
and Compliance standards.
4.2 Tasks outside projects
4.2.1 Assumes other duties as assigned by the Medical Science Director

Feeder roles:
・The person who meets the requirements above
Measures of Success:
・The context of clinical science input, including scientific risks, mitigations and setting right
expectation of clinical development POS, is properly understood by the internal governance
bodies for their quality decisions and by the internal stakeholders for the engagement.
・Optimum clinical science strategy is provided for optimum market access of the products within TA
portfolio
Education and Experience
Education and Degree
・Medical Doctor degree required
Education and Experience
・Doctor of Philosophy preferred
Experience
・Clinical practice as physician
・Planning of clinical development strategy and execution of clinical trials
・Negotiations with external experts and authorities
・Getting JNDA approval and supporting launch activities
Skills and Capabilities
Communication-related
・Communication skill
・Interview skill
・Negotiation skill
・Logical thinking
・Writing skill
・Presentation skill
Team working-related
・Meeting management
・Facilitation skill
・Project management
Reporting Relationship / Team Membership:
・Report to TA Medical Science Director
・Direct reports: None
Signed 
募集条件
Education and Experience
Education and Degree
・Medical Doctor degree required
Education and Experience
・Doctor of Philosophy preferred
Experience
・Clinical practice as physician
・Planning of clinical development strategy and execution of clinical trials
・Negotiations with external experts and authorities
・Getting JNDA approval and supporting launch activities

Skills and Capabilities
Communication-related
・Communication skill
・Interview skill
・Negotiation skill
・Logical thinking
・Writing skill
・Presentation skill

Team working-related
・Meeting management
・Facilitation skill
・Project management
Reporting Relationship / Team Membership:
・Report to TA Medical Science Director
・Direct reports: None 
勤務地
東京・大阪

7件中1~7件を表示しています。