LATAM Study Start-Up: Regulatory Submissions Lead

A clinical trial management firm in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join the Study Start-Up team. This role requires at least 4 years of experience in regulatory submissions and strong communication skills. Responsibilities include managing global start-ups, quality checks on submission documents, and preparing informed...

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...

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

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 and grow...

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 and grow...

Job 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...

**ALL CV´s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE CONSIDERED!** **Essential Functions**: - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings - Review and adapt study specific...

Start 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...

Study Start Up Associate II 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. Responsibilities: Proficient knowledge of ICON SOPs/WPs, ICH/GCP and...