Global Medical Affairs Research Grant Manager

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Santen Pharmaceutical

Site WebLinkedInTous les Emplois

1001 - 5000 employés

💊 Pharmaceutique

🏥 Santé

🏭 Fabrication

Pharmaceuticals • Healthcare • Manufacturing

Entreprise spécialisée dans l’ophtalmologie, Santen mène des activités de recherche, de développement, de marketing et de commercialisation de produits pharmaceutiques, de médicaments en vente libre (OTC) et de dispositifs médicaux. Santen est le leader du marché des produits pharmaceutiques ophtalmiques sur ordonnance au Japon et ses produits atteignent désormais des patients dans plus de 60 pays. Forte de connaissances scientifiques et de capacités organisationnelles développées au cours de ses 130 ans d’histoire, Santen propose des produits et des services qui contribuent au bien-être des patients, de leurs proches et, par extension, de la société.

Description

• Own and manage the end-to-end lifecycle of Investigator-Sponsored Studies (ISS/IST) and research grant programs • Coordinate proposal intake, scientific review, governance processes, contracting, milestone tracking, reporting requirements, and payments • Ensure studies comply with company policies, ethical standards, and applicable regulations • Maintain inspection-ready documentation and provide oversight throughout study execution • Provide operational support for Medical Affairs-sponsored evidence-generation activities across multiple regions • Manage Phase IV studies, observational research, registries, post-authorization studies, and real-world evidence initiatives • Monitor timelines, budgets, deliverables, risks, and study performance • Support dissemination of study outcomes through publications, presentations, and scientific communications • Partner with Clinical Development and Clinical Operations teams to support Phase III programs and transition into post-approval research • Contribute to evidence-generation planning, investigator engagement, and study feasibility activities • Build partnerships with investigators, academic institutions, healthcare professionals, research organizations, and key opinion leaders • Work with CROs and external vendors to ensure quality delivery and operational excellence

🎯 Exigences

• 5+ years of experience in Medical Affairs, Clinical Research, Clinical Operations, Evidence Generation, or a related field • Strong experience managing Investigator-Sponsored Studies (ISS/IST) and research grant programs • Expertise in research grant governance, review processes, contracting, milestone management, reporting, and payment oversight • Experience in Medical Affairs evidence generation, including Phase IV studies, registries, observational research, and real-world evidence programs • Experience collaborating with Clinical Development teams and supporting transition from Phase III clinical programs to post-approval research • Experience working with investigators, academic institutions, KOLs, CROs, and external research partners • Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, or another relevant scientific discipline • Strong working knowledge of GCP, ICH guidelines, and clinical research regulations • Fluent English communication skills • Advanced scientific degree (PhD, PharmD, MPH, MSc) preferred

🏖️ Avantages

• Flexible ways of working • Highly inclusive work environment • Competitive market-aligned base salary • Equal opportunity employer • Accommodation during the recruitment process if required