Trial Master File Associate
7 giorni fa
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.About this roleAs part of our CDSOphthalmology Trial Master File team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.The Trial Master File Associate is is part of the TMF Delivery Business Line within Clinical Development Services (CDS) and will function operationally as a member of the Study Team with the responsibility to organize, maintain and oversee the Trial Master File (TMF) according to company policies, SOPs, Work Instructions, regulatory requirements, TMF Functional Lead and PM delegation.Key ResponsibilitiesNotify study team that TMF is created and ready for document upload for eTMF or submission to pTMFDevelop TMF PlanProvide training on study specific TMF requirements, guidelines including TMF PlanPerform QC2 on documents and documents reconciliationProvide TMF Monthly Reports to PM, Line manager and Head of TMF DeliveryRegularly check TMF metrics, follow up on detected issues, ensure acceptable level of metricsEnsure TMF processes timely implementation and executionAdjusting study specific TMF Index/EDL in the relevant files/ system as directed by the PM (Project Manager)Ensure valid forms and templates are implemented and maintained in the assigned projectsCheck status of duplicates, documents in error, size and path length (if applicable), follow up on necessary corrections accordinglyCoordinate Monthly and Quarterly TMF Reconciliation by creating Action Plan and submitting relevant report on the statusEnsure TMF AoR completion and monitoring TMF
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Trial Master File Associate
16 ore fa
Turbigo, Italia TFS HealthScience A tempo pienoTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our CDSOphthalmology Trial...
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Turbigo, Italia TFS HealthScience A tempo pienoA global Contract Research Organization is seeking a Trial Master File Associate to manage the Trial Master File (TMF) within clinical development. Responsibilities include overseeing documentation upload, developing TMF plans, and providing training to the study team. Candidates should have 1-5 years experience in the CRO or pharmaceutical industry, with a...
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Global Clinical Trial Ops
7 giorni fa
turbigo, Italia Planet Pharma A tempo pienoA leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy, to provide operational support to the global clinical team. The role is vital in maintaining quality systems and documentation compliance. Ideal candidates will have a Bachelor's degree in a related field and be fluent in both English and Italian. Experience in...
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Global Clinical Trial Ops
16 ore fa
Turbigo, Italia Planet Pharma A tempo pienoA leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy, to provide operational support to the global clinical team. The role is vital in maintaining quality systems and documentation compliance. Ideal candidates will have a Bachelor's degree in a related field and be fluent in both English and Italian. Experience in...
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Clinical Trial Associate
7 giorni fa
turbigo, Italia Planet Pharma A tempo pienoPlanet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities.Key...
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Clinical Trial Associate
6 giorni fa
Turbigo, Italia Planet Pharma A tempo pienoPlanet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities. Key Responsibilities...
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Clinical Trial Associate
6 giorni fa
Turbigo, Italia Planet Pharma A tempo pienoPlanet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities. Key Responsibilities...
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Clinical Trial Associate
16 ore fa
Turbigo, Italia Planet Pharma A tempo pienoPlanet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities. Key Responsibilities...
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Global Clinical Trial Ops
17 ore fa
Turbigo (MI), Italia Planet Pharma A tempo pienoA leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy, to provide operational support to the global clinical team. The role is vital in maintaining quality systems and documentation compliance. Ideal candidates will have a Bachelor's degree in a related field and be fluent in both English and Italian. Experience in...
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Associate Clinical Trial Manager
16 ore fa
Turbigo, Italia Medpace A tempo pienoMedpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical...
