Senior Clinical Research Associate

Job SummaryAs a Clinical Research Associate Lead at PSI, you will oversee local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality, and study compliance on a country/regional level.Key ResponsibilitiesFacilitate regional projects as Lead Monitor and...

Job Overview:PSI is seeking a highly skilled and experienced Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for managing local monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety and well-being, data quality...

Clinical Research Associate Job Summary:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. This role will be responsible for conducting site visits to assess protocol and regulatory compliance, managing required documentation, and ensuring that data will pass international quality assurance audits.Key...

Job Title: Site Management Associate IJob Summary: We are seeking a highly skilled Site Management Associate I to join our international team at Psi Cro. This role will play a crucial part in the success of our clinical research projects, ensuring seamless communication, system maintenance, and document management.Main Responsibilities:•Communication and...

Job Title: Clinical Research Associate Lead About PSI:We are a leading provider of clinical research services, dedicated to advancing the field of medicine through high-quality research. Salary:$80,000 - $110,000 per annum, depending on experience Job Description:As a Clinical Research Associate Lead, you will be responsible for overseeing the management...

Job Summary:The Clinical Research Associate will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations, and PPD SOPs.Key Responsibilities:Conduct site visits to assess protocol and regulatory compliance and manage required...

Lead Clinical Research AssociateAbout PSI:PSI is a dynamic organization dedicated to advancing clinical research. Our team of experts works together to deliver high-quality projects and services to our clients.Salary Range: $70,000 - $90,000 per year, depending on experience and qualifications.Job Description:Role Overview:The Lead Clinical Research...

About the Role:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will play a vital role in ensuring the successful delivery of clinical trials.Job Summary:The Clinical Research Associate will be responsible for coordinating and conducting site...

Job SummaryAt MSD, we are seeking a Senior Clinical Research Associate to join our team.The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager, the person ensures compliance of study conduct with ICH/GCP and country regulations, Policies and procedures, quality standards...

Job Description OverviewThe Merck Gruppe - MSD Sharp & Dohme is seeking an experienced Clinical Research Associate to join our team as a Clinical Research Site Manager - Senior. As a key member of our global clinical operations team, you will be responsible for managing and overseeing the execution of clinical trials at assigned sites.Key...

Job OverviewPsi Cro is a dynamic, global company founded in 1995, bringing together over 2,800 driven individuals working on the frontline of medical science.Estimated Salary: $60,000 - $80,000 per yearJob DescriptionWe are seeking a highly organized Clinical Research Coordinator to join our international team. As the primary site contact point, you will be...

**Company Overview**ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence.We're proud to welcome you to join us on our mission to shape the future of clinical development.**About the Role**We are currently seeking a Clinical Trial Administrator to join...

Job OverviewWe are seeking a highly skilled Site Activation Specialist to join our team at IQVIA Argentina. The successful candidate 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 PSI CROWe are a global Contract Research Organization (CRO) with a commitment to developing our employees in their careers by providing tailored courses and mentoring. Our dynamic team is looking for an experienced Clinical Research Associate to train and coordinate junior CRAs on site.Job DescriptionHome-based position in Colombia, the role will...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country, in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards, and adverse event reporting requirements internally and externally.Key Responsibilities:Main Point of Contact (POC)...

Calling ALL Experienced Clinical LeadsThe Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality, and cost of delivery and in...

Job Overview">We are seeking an experienced Senior Clinical Data Operations Manager to join our Global Data Operations team at MSD. In this role, you will lead a team of senior clinical data managers and clinical data managers in operations tasks, both strategic and tactical in nature, within a Data Management Center.

About BOG Fortrea Colombia Ltda.As a leading global contract research organization (CRO), Fortrea is dedicated to delivering clinical development, patient access, and technology solutions across various therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, we are transforming drug and device development for partners and...

OverviewCDS Fortrea Inc. is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.SalaryThe estimated salary for this position is $85,000 - $110,000 per year.Job DescriptionThis Senior Clinical Trials Coordinator role involves serving as the primary contact for project teams and...

Company OverviewIqvia Argentina is a leading healthcare consulting firm that helps clients navigate the complexities of clinical research. We are seeking a highly skilled and experienced Site Activation Manager to join our team.Salary$65,000 - $80,000 per annum, depending on experience.Job DescriptionWe are looking for a talented Site Activation Manager to...