Clinical Study Start-Up Associate: Regulatory Submissions

OverviewStudy 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...

JOB_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...

A leading healthcare intelligence organization in Buenos Aires seeks a Study Start Up Associate I. You will support regulatory submissions, coordinate approvals, and assist study teams in document development. A bachelor's degree in life sciences is required, along with strong attention to detail and communication skills. Join a diverse team committed to...

Study Start Up I 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 Study Start Up Associate I to join our diverse and...

Study Start Up Associate I, China, office based 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. What you will be doing Assisting in the...

Study Start Up Associate I JR093872 Site: Buenos Aires - Argentina At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and...

Site Specialist II, Study Start Up 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 Site Specialist II (Study Start Up...

Overview 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 study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

Our 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...

**Trial and site administration**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply & non-clinical supply management, in collaboration with other country roles - Manage Labeling requirements and...