Regulatory Start-Up Expert

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...

We are looking for a highly skilled Project Start Up Expert to join our team at Beiersdorf S.A. (Argentina). In this role, you will be responsible for performing start up and site activation activities, working closely with sponsors and project teams to ensure successful project delivery.The ideal candidate will have experience with external commerce in...

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...

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 the RoleWe seek a talented Regulatory and Start-Up Specialist to join our Argentina-based team. In this role, you will perform tasks associated with Site Activation (SA) activities, adhering to local and international regulations, SOPs, and project requirements.Main Responsibilities:Act as SPOC for assigned studies, providing support to investigative...

Key QualificationsAt least 4 years of regulatory submissions/start-up management experience (leading regulatory/start-up project teams);Knowledge and experience of Clinical Trial Applications within LATAM;Strong oral and written communication skills;Team-oriented approach and strong leadership skills;Willing to work in an office-based model;Fluency 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...

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 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...

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...

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...

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...

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...

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 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...

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...

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...