Study Start Up Associate I

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 fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

Study Start Up Associate II - Chile - Homebased 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: - Coordinating and...

Unleash Your Potential It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward. Join IQVIA and see where...

Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, remote Regulatory Submissions Manager to join our Study Start Up team in Chile! This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global start-up; Perform quality...

Help create a healthier world: START RIGHT HERE AT IQVIA. Proficiency in English, both verbally and written are necessary. Please submit resume in English. Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures...

Help create a healthier world: START RIGHT HERE AT IQVIA. Proficiency in English, both verbally and written are necessary. Please submit resume in English. Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures...

GENERAL - Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client, as applicable. - Serve as client’s contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working relationship with client’s project teams. - Monitor and control start up...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience,...

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.Job OverviewDirect and manage the...

Santiago, Chile | Full time | Home-based | R1504165Job available in additional locationsIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that...