We're Hiring: TMF Specialists (2 Open Positions)About the RoleWe are looking fortwo detail-oriented TMF Specialiststo join our growing Clinical Operations team.Manage and maintain electronic Trial Master Files (eTMF) throughout the study lifecycle.Review, classify, and file essential clinical trial documents.Conduct TMF quality checks and completeness reviews.Track missing or overdue documents and follow up with study teams.Support TMF reconciliation activities and inspection readiness.Collaborate with Clinical Operations, Regulatory Affairs, Quality Assurance, and external partners.Generate TMF metrics, reports, and study documentation status updates.Assist during audits and regulatory inspections.Contribute to continuous improvement initiatives and TMF best practices.Bachelor's degree in Life Sciences, Pharmacy, Biology, Health Sciences,



or a related field.ExperienceApproximately2 years of experiencein:TMF ManagementClinical OperationsClinical ResearchDocument Management within the Life Sciences industryGood understanding ofICH-GCPand clinical trial documentation.Experience with eTMF platformsExcellent organizational and documentation skills.Strong attention to detail.Ability to manage multiple priorities in a fast-paced environment.Strong communication and stakeholder management abilities.Fluent English (written and spoken) is required.Additional languages are a plus.What We OfferCompetitive salary packageInternational and multicultural work environmentOngoing learning and professional development opportunitiesCareer growth within Clinical Research and Clinical OperationsCollaborative and supportive team culture#J-18808-Ljbffr

📌 Trial Master Files Specialist (Madrid)
🏢 CliniRx
📍 Madrid