Study Start Up Manager

Overview Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Founded more than 47 years ago as Emmes, we entered the US government leading clinical research arena before expanding into public‑private partnerships and commercial biopharma. Our leading capabilities cover...

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...

A leading clinical research organization is seeking a Study Start-up Associate Senior in Rincón de los Sauces, Argentina. This role is vital for coordinating regulatory submissions and ensuring compliance with local and global requirements in clinical trials. Ideal candidates will have over 6 years of experience in regulatory affairs across multiple...

A leading healthcare organization is seeking a Study Start Up Associate II to lead clinical trial initiation, ensuring regulatory compliance and collaboration with stakeholders. The ideal candidate holds a Bachelor's degree in life sciences, with at least 2 years of experience in clinical research. ICON offers a supportive work environment and attractive...

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 Senior Clinical Research Associate (CRA) to join our diverse and...

Overview The Regulatory and Start-Up Specialist 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. May also include maintenance activities. Responsibilities...

Quality Control Analyst In line with the process of designing and launching global clinical research studies, conduct independent quality control (QC) reviews and ensure adherence to study set‑up processes and procedures during start‑up and amendment phases. Responsibilities include reviewing source documentation and database configuration against...

The R egulatory and Start-Up Specialist 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. May also include maintenance activities. Essential Functions Under...

Sr Global Trial Manager - Sponsor Dedicated IQVIA’s mission is to accelerate innovation to help create a healthier world – and delivering on this ambition requires the right connections between our capabilities, expertise, and people. Every day, we work together to drive healthcare forward in ways both big and small, helping customers solve problems and...

Sr Global Trial Manager - Sponsor Dedicated IQVIA’s mission is to accelerate innovation to help create a healthier world – and delivering on this ambition requires the right connections between our capabilities, expertise, and people. Every day, we work together to drive healthcare forward in ways both big and small, helping customers solve problems and...