Senior Clinical Study Start-Up Lead

A global biopharmaceutical company is seeking a Senior Specialist Country Study Start Up to drive start-up and maintenance activities for clinical studies. The ideal candidate will have at least 3 years of experience in clinical research and strong expertise in site activation plans. Responsibilities include coordinating with IRB/EC sites, maintaining...

Senior Specialist Country Study Start Up AbbVie Company Description The Sr. Specialist, Country Study Start Up proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. The Sr. Specialist, Country SSU is responsible and accountable for on-time,...

A leading healthcare clinical research organization in Buenos Aires seeks a Manager, Study Start-Up. In this role, you will manage the end-to-end study start-up process, overseeing a team and ensuring compliance with regulations. Ideal candidates will have a background in life sciences, significant clinical trial experience, and strong leadership skills. The...

Study Start up Lead **Category**:Clinical Development**Location**:Vicente Lopez, Buenos Aires, AR- Are you ready for a life-changing career at Novo Nordisk Argentina? Join us.- Working at Novo Nordisk is never just a job, it is an opportunity to have a life-changing career - you grow professionally.**The Position**Activities and Responsibilities** -...

A 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...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO Site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is...

A leading clinical research organization in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join their Study Start Up team. This role involves managing all aspects of global start-up and requires at least 4 years of experience in regulatory submissions and strong leadership skills. You will collaborate with teams to contribute to...

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...

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 CRA 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...