Descripción de la oferta
Overview
In this role you provide medical input and oversight for clinical development programs within Global Clinical Development, collaborating with cross-functional teams and GCPL/line managers. You may deputize on defined tasks, lead medical data review, and support protocol development, amendments, and scientific content. You will engage with Ethics Committees, investigators, and external KOLs to advance program delivery and publications, contributing to a patient-centric dermatology portfolio.
Compensaciones / BeneficiosTop Employer SpainTop Employer Germany (first time)people-centric cultureopportunities for professional development
ResponsabilidadesSupport GCPL and Clinical Development Scientist in designing development plans and studiesBack up GCPL responsibilities for defined tasks under supervisionContribute to study synopsis, protocol and amendments with GCPLs and CDSReview scientific content of protocols, amendments, CSRs, ICF, CRF and related documents (IB, briefing packages, ISE, ISS, publication)Deputize GCPL as a member of the Global Project TeamProvide medical support to Study Team for Ethics Committees and investigatorsLead medical data review including eligibility and safety dataSupport protocol deviation review medicallyPartner with CDS and Clinical Operations to support study delivery (enrollment, eligibility, protocol violations, amendments)Assist GCPL and CDS in data analysis, data review and publication content after study resultsRemain a core member of the Clinical Study TeamBuild relationships with external KOLs
Requisitos principalesMedical degreeDermatology specialty is a plusPrior experience in clinical studies (sub-investigator or industry/CRO)Fluency in English (written and spoken)Proficiency with MS OfficeStrong communication and presentation abilitiesLeadership and influence to drive consensusAnalytical and problem-solving mindsetMS OfficeMedical data reviewClinical study documentation review
