Reg & Start Up Manager - Sponsor Dedicated

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...

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...

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...

Job Summary: We are seeking a highly motivated Clinical Trial Start-Up Specialist to join our team. As a key member of our start-up group, you will be responsible for ensuring the timely and successful activation of clinical trials in countries around the world.Key Responsibilities:Oversee and lead country study start up (SSU) activities, collaborating with...

Techunting is a dynamic company in an ever-changing industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection.As a key member of our clinical development department, you will be responsible for...

Job Description: As a Global Study Coordinator - Start-Up, you will play a critical role in the successful launch of clinical trials in countries worldwide. Your primary responsibility will be to oversee and lead country study start-up activities, working closely with cross-functional teams to ensure timely and efficient site activation.Key Tasks:Collect and...

Job SummaryWe are seeking an experienced Study Start-Up Specialist to join our team at Novo Nordisk Argentina.About the RoleDeveloping functional short and long-term strategic plans for Study Start-Up (SSU) in accordance with global/regional KPIs.Building and managing high-performing start-up teams to ensure timely trial deliverables.Establishing and...

Job DescriptionEnsure successful execution of start-up and maintenance activities for assigned sites and studies.Establish country/site activation plans and priorities, including risk assessment and mitigation plans.Proactively identify and communicate issues impacting delivery and propose solutions.As a US Start-Up Coordinator, you will play a key role in...

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...

Study Start up Lead Category: 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 Responsibilities Developing Study Start-Up...

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...

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...

Job DescriptionThe Sr. 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 guidelines.This role is responsible for ensuring adherence to standard...

About This RoleWe are seeking a highly skilled Regulatory and Start-Up Specialist to join our team in Argentina. As a key member of our Site Activation team, you will be responsible for ensuring that all site activation activities are performed in accordance with applicable regulations, SOPs, and project requirements.Responsibilities:Site Activation: Perform...

The Ideal CandidateBachelor's Degree required, preferably in a health care or scientific field.A minimum of 1-2 years of clinical research experience and +1 year of study start-up management experience supporting US.Advanced English level.You should have good analytical and critical thinking skills, as well as excellent communication and interpersonal...

About the OpportunityThis is an exciting opportunity for a highly motivated and organized individual to join our Clinical Operations team at Amazon Web Services Argentina as a Clinical Trial Contract Specialist. As a key member of the team, you will play a critical role in the study start-up and clinical trial management processes.Main...

About UsWe are a leading company in the industry, dedicated to providing high-quality services to our clients.We are looking for talented individuals who share our values and are passionate about delivering exceptional results.If you are a motivated and results-driven professional, we encourage you to apply for this exciting opportunity.

We are seeking a Research Site Manager to join our team of experts. As a Research Site Manager, you'll be responsible for overseeing the conduct of clinical studies at research sites. This includes setting up and monitoring study activities, preparing regulatory submissions, and balancing sponsor generated queries efficiently.Key ResponsibilitiesOversee the...

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...

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...