Clinical Research Coordinator

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...

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...

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...

Job SummaryJoin Medpace in our Buenos Aires office We are currently seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous...

Clinical Trials CoordinationWe are looking for a talented Clinical Trial Coordinator to support our clinical trials operations at IQVIA Argentina. In this role, you will work closely with internal stakeholders and external partners to set up studies and data integrations within sample tracking software systems.Key FunctionsAssist in the development of...

Job OverviewMilestone One is a dynamic, global company founded in 1995, dedicated to bringing new medicines to those who need them. As a Site Management Associate I, you will play a crucial role in clinical research projects, streamlining communication and managing documents & information.You will be the main point of contact between site personnel and CRA...

Job Description:The Global Clinical Logistics Coordinator will be responsible for managing global clinical supplies for multiple projects simultaneously. This includes coordinating and managing complex studies, handling client consultations, and serving as the primary point of contact between clients, project teams, vendors, and study...

Job OverviewThe Project Coordinator - Clinical Supply Chain is responsible for supporting 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.ResponsibilitiesSupport clinical supplies lifecycle for multiple...

Job OverviewWe are seeking a highly skilled Clinical Project Coordinator to join our team in the LATAM region. As a key member of our Global Clinical Supplies team, you will be responsible for providing overall global coordination of the entire clinical supplies lifecycle for assigned projects.The ideal candidate will have a strong understanding of global...

About the RoleThe Supply Chain Project Coordinator - Global Clinical is responsible for coordinating the clinical supplies lifecycle for multiple projects simultaneously. This role requires strong analytical skills and attention to detail, as well as excellent communication and interpersonal skills.ResponsibilitiesCoordinate clinical supplies lifecycle for...

The Clinical Study Assistant will provide administrative support for clinical trials at IQVIA Argentina. Your key responsibilities will include assisting investigators and site staff, verifying research study information, and preparing research study files.Main DutiesAssist investigators and site staff with clinical research activitiesVerify and correct...

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 OverviewPerform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.Essential FunctionsProvide clinical research support to investigators and site staff, includingVerify and/or correct research study...

**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...

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...

Overview:We are seeking a highly skilled Global Clinical Supply Chain Coordinator to join our team. In this role, you will be responsible for coordinating global clinical supplies lifecycle for assigned projects, including managing complex studies requiring primary and/or secondary packaging and labeling design, drug projections, distribution, returns,...

Senior Clinical Research Associates play a vital role in ensuring the success of our clinical trials. As a key member of our team, you will be responsible for coordinating activities, monitoring studies, and maintaining accurate documentation.The Job DescriptionSubmit protocol and consent documents for ethics/IRB approval, and prepare regulatory submissions...

We are seeking a Senior Project Coordinator, Global Clinical Supplies to join our team. As a key member of our Global Clinical Supplies team, you will be responsible for providing support to senior project managers and coordinating the entire clinical supplies lifecycle for projects assigned.Key Responsibilities:Assist in the development of project-specific...

About the Role:We are seeking a highly skilled Programmer and Analyst for Clinical Trials to join our team at Innovaderm Research Inc.The successful candidate will lead the programming activities for various purposes, including data listings for review, Safety Review Listings, Centralized Monitoring Listings, and Reports.This position requires strong...

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...