Lead Clinical Trial Operations Manager Jobs in Japan

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment ap...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

ABOUT THE ROLE日本におけるホテルポートフォリオの拡大をリードする開発ディレクターを募集しています本ポジションはAccorの全ブランドを対象にさまざまな契約形態運営受託フランチャイズレジデンスやプロジェクトタイプホテルリゾート長期滞在型ブランドレジデンス複合開発に関する開発案件の獲得交渉契約締結までを担う...

Job DescriptionPOSITION OVERVIEW:The Associate Director of the Regulatory Affairs (RA) is responsible for the management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA division of Animal Health in Japan. The position requires a combination of scientific kn...

Work Flexibility: Hybrid or OnsiteAbout the job:The role exists to oversee entire Medical Business Unit and drive the team to ensure the attainment of financial and operational goals in support of Stryker Japans overall financial and strategic objectives. The position holder will plan direct and coo...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Are you ready to make a difference in the world of regulatory operations At Regeneron were seeking a Manager of Regulatory Submission Project Management (RSPM) to lead the strategic planning and execution of regulatory milestones across our therapeutic areas. This is your chance to join a collaborat...

Job OverviewThe MSL role is field based customer facing role activities should be Key medical expert (KME) focused with the intent to maximize medical one on one interactions with HCPs. Over70% field-related activities (face to face and virtual) is expected in the roleActs as a scientific expert kno...

Medical Science LiaisonMedical AffairsTokyo JapanAre you passionate about advancing patient care through scientific communication Do you thrive on building meaningful relationships with healthcare professionals and key opinion leaders If so we have an exciting opportunity for you to join our team as...

The Creative team provides customers with original relevantand contemporary industry-uniquecombination of consumer research proprietarydataandthree decades oftrendreportingexperience the teamdeliversactionableinsightsthatguidecustomersto the visual content that connects with consumers. Closelycolla...

As part of our global expansion we are now looking for in-country regulatory professionals to join our growing global regulatory team. This is an exciting opportunity to demonstrate your knowledge in leading regulatory processes for biological products and regenerative medicines in Japan and to buil...

Job SummaryResponsible for Quality Assurance (QA) and Quality Control (QC) operations in Biogen Japan to ensure that all commercial products comply with relevant regulations namely Good Quality Practice Good Manufacturing Practice and Biogen Quality Management System. Accountable for assuring releas...

Pipeline Medical Science Liaison (MSL) Nephrology (Fixed Term Contract role)About This Role:As a Pipeline MSL in Nephrology you will be an integral part of our medical affairs team focusing on enhancing our scientific credibility with clinical investigators and key scientific institutions. Your rol...

ジェンマブは革新的な抗体医薬の開発に注力し患者さんの生活を改善することに力を尽くしています私たちはextranotordinary な未来を共に築くことを使命とし革新的な抗体製品の開発や人々を感動させる抗体医薬品でがんやその他の深刻な病に苦しむ患者さんの生活を根本的に変え治療の未来を切り拓いていますジェンマブは思い...

Summary:The Regional Medical Affairs Manager / Sr Regional Medical Affairs Manager will be responsible for facilitating scientific exchange and clinical support for Gossamers clinical studies and will engage with clinical study sites investigators and study personnel to encourage fast study start up...

Clinical Trial Psych Rater - Japanese SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We partner with t...