FSP Regulatory and Start Up Specialist in Argentina

We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based roleWhat You´ll DoPerform 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...

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. Developing professional...

Job OverviewAbout IqviaWe are a leading healthcare consulting company that helps pharmaceutical companies navigate the complexities of global regulatory environments.Job DescriptionThe Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation activities in accordance with applicable local and/or international...

Role Description Study-Start-Up/QC Specialist:Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to...

IQVIA Regulatory & Start Up Specialist, cFSP - US Support Location: Argentina - Full Home Based rolePurpose: The RSU Specialist 1 proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country: US.Responsibilities: Ensuring successful and on time and quality execution...

Company OverviewIQVIA is a leading provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to helping our clients navigate the complexities of the healthcare landscape and improve patient outcomes.Job DescriptionThe Regulatory & Start Up Specialist will be responsible for supporting...

IQVIARegulatory & Start Up Specialist, cFSP - US SupportLocation: Argentina - Full Home Based rolePurpose: The RSU Specialist 1 proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country: US.Responsibilities:Ensuring successful and on time and quality execution of...

Job DescriptionAbout IqviaWe are a leading healthcare consulting company that helps pharmaceutical companies navigate the complexities of global regulatory environments.Key ResponsibilitiesThe Regulatory and Start-Up Specialist will be responsible for:Developing professional individual contributor who works under moderate oversight and supervision.Ensuring...

Regulatory Document Management SpecialistFeverUpWe are looking for a highly skilled Regulatory Document Management Specialist to join our team. In this role, you will be responsible for ensuring the completeness and accuracy of site essential document packages and site regulatory packages.This includes reviewing and approving site documentation, conducting...

About FeverupWe are a leading company in the Pharmaceutical /CRO industry, dedicated to delivering high-quality services to our clients. Our team is passionate about innovation and excellence, and we are seeking a talented Senior Study Start-Up Expert to join us.As a Senior Study Start-Up Expert, you will be responsible for ensuring the smooth execution of...

Job SummaryOur 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 AiresThis position plays a key role in the clinical trial management process at Medpace.If you want an exciting career where you use your previous expertise and can...

Job OverviewThe Regulatory & 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 guidelines. This role may also include maintenance activities.Key...

Reg & Start Up Manager – Sponsor DedicatedDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work and resources.You will:Oversee the execution of Site Activation and Maintenance for assigned projects...

About the JobWe are seeking a highly skilled Regulatory Document Specialist to join our team at Feverup. As a key member of our site initiation and activation team, you will be responsible for ensuring the completeness of Site Essential Document Packages as well as the Site Regulatory Packages (SRP) required to achieve site initiation and activation...

Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion,...

At Syneos Health Clinical, we are at the forefront of bringing life-saving therapies to patients. Our clinical research services team is comprised of highly skilled professionals who work together to develop innovative solutions for the world's most challenging health concerns.We are vital links between an idea for a new medicine and the people who need it....

Sr. Site Activation Specialist in ArgentinaIQVIAThe Sr. Site Activation 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...

Study Start up LeadCategory: Clinical DevelopmentLocation: Vicente Lopez, Buenos Aires, ARAre 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 PositionActivities and ResponsibilitiesDeveloping Study Start-Up...

Parexel is hiring a Program Specialist in Argentina to support our FSP team.An FSP Program Specialist proactively cooperates with the FSP Operations Leads, FSP General Managers, FSP Program Leads, and FSP Functional Leads on program tasks and coordinates team activities in areas owned by the PS.Understands PS role impact on program success, particularly on...

We are committed to developing our employees in a continuous learning culture, where every experience adds to your professional development. As a Regulatory Compliance Specialist, you will play a critical role in ensuring the integrity of our clinical trials and adherence to regulatory requirements.Your key responsibilities will...