Senior Clinical Research Specialist

About the Role:We are seeking an experienced Senior Clinical Supply Specialist to join our team. As a key member of our Global Clinical Supplies team, you will be responsible for managing complex clinical supplies studies, providing consultation services to clients, and serving as the primary point of contact between clients, project teams, vendors, and...

Job Summary: The Senior Clinical Research Associate II is responsible for site monitoring and management of clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. This role requires a strong understanding of clinical research principles and regulatory requirements. As a Senior CRA II, you will be...

At IQVIA LLC, we are seeking a Senior Trade Specialist to join our team. As a key member of the CSA team, you will be responsible for importations and exportation activities in Argentina.Skillset:Import and export processesClinical research experienceInternational trade regulationsAbout the Role:The Senior Trade Specialist will ensure adherence to standard...

At Inclusion Cloud, we are committed to delivering innovative solutions in medical science. As a Senior Clinical Research Associate II (Lead Monitor), you will play a vital role in facilitating regional projects and overseeing study activities.Key Responsibilities:Facilitate regional projects as Lead Monitor and supervise study activities, timelines, and...

The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and Programmer will be responsible to gather, understand and analyze the needs reported by the Data...

Job Description: We are seeking an experienced Senior Clinical Research Associate II to join our team at St Andrew's Scots School. As a Senior CRA II, you will be responsible for conducting on-site monitoring activities and managing clinical sites. This role requires a strong understanding of clinical research principles and regulatory requirements.About the...

The Senior Clinical Research Associate (CRA) plays a crucial role in the planning, execution, and management of clinical trials at IQVIA Argentina.This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research...

QualificationsTo be considered for this role, you must possess:A Bachelor's Degree in life sciences.+3 years of clinical research experience within the regulatory area in Argentina, specifically in local submissions, ICF customization, and presentations to ethics committees and ANMAT.Fluent English language skills, including written and oral...

Company OverviewIQVIA is a leading provider of healthcare consulting and technology solutions. We are dedicated to helping our clients navigate the complexities of clinical research and improve patient outcomes.Job DescriptionClinical Research CoordinatorWe are seeking an experienced Clinical Research Coordinator to join our team in Quilmes centro, Provincia...

**Job Overview**IQVIA Argentina seeks a highly skilled and detail-oriented Clinical Trials Support Specialist to provide administrative support for clinical trials. This role involves assisting investigators and site staff, verifying research study information, and preparing research study files.Key ResponsibilitiesProvide clinical research support to...

Senior Clinical Research Associate - Sr CraLabcorpThe Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines.The Sr CRA II assures the implementation of project plans as...

The Senior Clinical Research Associate will play a crucial role in the planning, execution, and management of clinical trials.This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.Responsibilities may...

Job OverviewWe are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at IQVIA. As a key member of our clinical research support team, you will be responsible for providing administrative assistance to investigators and site staff, ensuring the smooth conduct of clinical trials.Key ResponsibilitiesProvide Research...

We are seeking a skilled and organized individual to fill the role of Administrative Assistant - Clinical Research. As an Administrative Assistant, you will provide administrative support for clinical trials, including assisting investigators and site staff, verifying research study information, and preparing research study files.Key ResponsibilitiesProvide...

AgileEngine is a clinical research organisation driven by excellence in delivering high-quality services to our clients. We're committed to advancing and improving patients' lives through innovative solutions.The RoleWe are seeking a highly motivated Senior Clinical Research Associate to coordinate activities, monitor studies, and maintain accurate...

Senior Clinical Research Associate - Sr CraLabcorpThe Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of project plans as...

As a Research Site Coordinator - Clinical Trials, you will play a crucial role in supporting the success of clinical trials at IQVIA Argentina. Your responsibilities will include providing clinical research support to investigators and site staff, verifying research study information, and preparing research study files.Main DutiesAssist investigators and...

About the RoleAs a Research Assistant - Clinical Trials at IQVIA, you will play a critical role in supporting the conduct of clinical trials. This position involves working closely with investigators and site staff to ensure the successful execution of research studies.Main ResponsibilitiesSupport Research ActivitiesVerify and correct research study...

Job SummaryThe Global Clinical Operations Specialist is responsible for managing the clinical supplies lifecycle for multiple projects simultaneously. This role requires strong organizational skills and attention to detail, as well as excellent communication and interpersonal skills.ResponsibilitiesManage clinical supplies lifecycle for multiple projects...

Job OverviewMatcheamos is seeking a highly skilled Regulatory & Start Up Specialist to join our team in a Home Based role.About the RoleWe are looking for an experienced professional to perform tasks at a country level associated with Site Activation (SA) activities. The successful candidate will ensure adherence to standard operating procedures (SOPs), Work...