Reg & Start Up Spec 2
hace 2 semanas
We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based role What You´ll Do Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. - Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. - Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. - Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members. - Prepare site regulatory documents, reviewing for completeness and accuracy. - Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. - Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines. - Provide local expertise to SAMs and project team during initial and on-going project timeline planning. - Perform quality control of documents provided by sites. - May have direct contact with sponsors on specific initiatives. What Will Help You Succeed - +2 years clinical research experience submitting clinical procedures to the MoH (ISP). - Health Sciences degree - +1 year experience handling the "FEFYM" and “CABA” portal when submitting clinical procedures - Advanced command of English language. - Desirable experience in imports/exports that correspond to activities subsequent to the authorization of a clinical protocol in the country. - Desirable experience in contract negotiations with research sites. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
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Start-up Specialist
hace 3 semanas
Buenos Aires, Argentina Remoteco A tiempo completoRole Description Study-Start-Up/QC Specialist: Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to...
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Start Up Manager
hace 3 semanas
Buenos Aires, Argentina ICON A tiempo completoStart Up Manager ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Manager, Study Start‑Up to join our diverse and...
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Start Up Manager
hace 2 días
Buenos Aires, Buenos Aires C.F., Argentina IRE A tiempo completoStart Up ManagerICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Manager, Study Start-Up to join our diverse and dynamic...
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Fsp - Regulatory and Start Up Specialist 2 - Arg
hace 4 semanas
Buenos Aires, Argentina Wimbush & Associates, Inc. A tiempo completoFsp - Regulatory and Start Up Specialist 2 - Arg IQVIA Job Overview The Regulatory & Start Up Specialist 2 will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines....
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Clinical Study Start-Up
hace 3 semanas
Buenos Aires, Argentina Remoteco A tiempo completoA global clinical trials organization is seeking a Study Start-Up/QC Specialist in Buenos Aires, Argentina. The ideal candidate will oversee clinical trial start-up activities and perform quality reviews of essential documents to ensure compliance with ICH-GCP and local regulations. This role requires a Bachelor's degree and at least 2 years of clinical...
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Study Start Up Manager
hace 1 semana
Buenos Aires, Argentina Medpace A tiempo completoOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow...
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Study Start Up Manager
hace 6 días
Buenos Aires, Buenos Aires C.F., Argentina Medpace A tiempo completoOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-basedRegulatory Submissions Managerto join our Study Start Up team in Buenos Aires This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your...
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Study Start-up Associate Senior
hace 1 semana
Buenos Aires, Buenos Aires C.F., Argentina Emmes Global A tiempo completoOverviewStudy Start-up Associate SeniorLATAM RemoteEmmes Group: Building a better future for us all.Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the...
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Study Start Up Manager
hace 3 semanas
Buenos Aires, Argentina International Flavors & Fragrances A tiempo completoJob Summary: Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full‑time, office‑based Regulatory Submissions Manager to join our Study Start‑Up team in Buenos Aires! This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous...
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Study Start-up Associate Senior
hace 1 semana
Buenos Aires, Buenos Aires C.F., Argentina Emmes Group A tiempo completoJOB_DESCRIPTION.SHARE.HTMLCAROUSEL_PARAGRAPHJOB_DESCRIPTION.SHARE.HTMLMexico City, Mexico; Buenos Aires, Argentina; Sao Paulo, BrazilLegal / Regulatory/ComplianceYesRegular Full-Time2730Emmes Globalmail_outlineGet future jobs matching this searchorOverviewJob DescriptionStudy Start-up Associate SeniorLATAM RemoteEmmes Group: Building a better future for us...