Regulatory Specialist for Clinical Research Start-ups

About this role:We are seeking a highly skilled Clinical Research Associate to join our Global Clinical Operations team. As a Clinical Research Associate, you will play a critical role in supporting the start-up and management of clinical trials across various regions.Key responsibilities:Conduct site start-up activities, including ethics committee...

About this role:We are seeking a highly skilled Clinical Research Associate to join our Global Clinical Operations team. As a Clinical Research Associate, you will play a critical role in supporting the start-up and management of clinical trials across various regions.Key responsibilities:Conduct site start-up activities, including ethics committee...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Boston Scientific Corporation. As a Clinical Research Associate, you will play a critical role in the preparation and approval of regulatory documents, ensuring compliance with service level agreements, legal and regulatory standards, and applicable company policies...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Boston Scientific Corporation. As a Clinical Research Associate, you will play a critical role in the preparation and approval of regulatory documents, ensuring compliance with service level agreements, legal and regulatory standards, and applicable company policies...

Clinical Trial Support Specialist, Dedicated to a Single Sponsor Job Overview: The Clinical Trial Assistant (CTA) is responsible for performing essential administrative functions in collaboration with Clinical Research Associates (CRAs) and the Regulatory and Start-Up teams. This role is crucial for ensuring the accurate and complete delivery of the...

Clinical Trial Support Specialist, Dedicated to a Single Sponsor Job Overview: The Clinical Trial Assistant (CTA) is responsible for executing daily administrative tasks in collaboration with Clinical Research Associates (CRAs) and the Regulatory and Start-Up teams. This role is crucial for ensuring the comprehensive and precise delivery of the Trial...

Job OverviewWe are seeking a highly skilled Regulatory and Start Up Specialist 2 to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard...

Job OverviewWe are seeking a highly skilled Regulatory and Start Up Specialist 2 to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard...

Job SummaryWe are seeking a highly skilled Clinical Trial Activation Specialist to join our team at Icon Clinical Plc. As a Clinical Trial Activation Specialist, you will be responsible for advancing clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution.Key...

Job SummaryWe are seeking a highly skilled Clinical Trial Activation Specialist to join our team at Icon Clinical Plc. As a Clinical Trial Activation Specialist, you will be responsible for advancing clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution.Key...

{"h1": "Study Start Up Associate II - Netherlands, Utrecht", "p": "At ICON, we're proud to foster an inclusive environment driving innovation and excellence. We're seeking a Study Start Up Associate II to lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and...

About the RoleWorldwide Clinical Trials is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management, and study...

About the RoleWorldwide Clinical Trials is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management, and study...

Job OverviewWe are seeking a highly skilled Regulatory and Start Up Specialist 2 to join our team at IQVIA. In this role, you will be responsible for performing 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...

Job OverviewWe are seeking a highly skilled Regulatory and Start Up Specialist 2 to join our team at IQVIA. In this role, you will be responsible for performing 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...

**About the Role**From Strategy to Operational ExcellenceThe Clinical Research Medical Advisor provides clinical development and indication expertise specific to the Country/Cluster, and together with the clinical trial operations team, drives the execution of clinical trials with high quality and within planned timelines:**Key Responsibilities**Validates...

**About the Role**From Strategy to Operational ExcellenceThe Clinical Research Medical Advisor provides clinical development and indication expertise specific to the Country/Cluster, and together with the clinical trial operations team, drives the execution of clinical trials with high quality and within planned timelines:**Key Responsibilities**Validates...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials, LLC. As a key member of our Clinical Operations team, you will play a vital role in ensuring the success of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management,...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials, LLC. As a key member of our Clinical Operations team, you will play a vital role in ensuring the success of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management,...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials. As a key member of our Clinical Operations team, you will play a vital role in ensuring the successful execution of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site...