Clinical Research Associate

{"title": "Clinical Research Associate", "content": "Job SummaryCDS Fortrea Inc. is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for monitoring clinical sites, maintaining study files, and conducting pre-study and initiation visits. You will also be responsible for ensuring...

Clinical Research Opportunities at PSI CRO **About the Role** As a Clinical Research Associate at PSI CRO, you will have the opportunity to work on a variety of clinical studies in different therapeutic indications. Our team is committed to delivering high-quality results and providing a supportive environment for our employees to grow and develop in their...

About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead the execution of clinical trials in our region. As a key member of our team, you will be responsible for managing trial operations, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to...

About PSI CROPSI CRO is a leading Contract Research Organization with over 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering high-quality and on-time services across a variety of therapeutic indications.Job SummaryWe are seeking a highly skilled Clinical...

About PSI CROPSI CRO is a leading Contract Research Organization with over 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering high-quality and on-time services across a variety of therapeutic indications.Job SummaryWe are seeking a highly skilled Clinical...

{"title": "Clinical Assessment Technologies Department", "description": "**About the Role**Worldwide Clinical Trials is seeking a skilled Clinician to join our Clinical Assessment Technologies Department. As a Clinician, you will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.**Key...

{"h1": "Clinical Research Associate", "p": "At ICON, we are committed to advancing human health through innovative clinical research. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing expert advice and guidance to our team members.Your key responsibilities will include:* Acting as an...

Job OverviewWe are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team at IQVIA. As a Senior Clinical Research Associate, you will be responsible for ensuring that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key...

Key Responsibilities:Manages clinical investigational sites, ensuring compliance with regulatory requirements and protocol guidelines.Key Accountabilities:Trains and directs investigators and site staff on clinical trial protocols and procedures.Reviews and verifies clinical documentation to ensure accuracy and completeness.Maintains drug accountability and...

{"Job OverviewAs a Senior Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Your expertise will be utilized to drive site recruitment plans, administer protocol and related study training, and...

About the RoleWe are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team at ICON. As a Senior Clinical Research Associate, you will play a key role in the success of our clinical trials by providing expert advice and guidance to less experienced colleagues.Key ResponsibilitiesExpert Advisor: Act as an expert advisor...

About the RoleWe are seeking a highly organized and detail-oriented Clinical Operations Associate to join our team at Worldwide Clinical Trials. As a key member of our Clinical Assessment Technologies group, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesTrack and manage rater experience...

About the Role:The Clinical Research Associate plays a critical role in ensuring the integrity and validity of clinical research data. As a key member of the research team, you will be responsible for managing and supporting clinical research sites, monitoring clinical data to ensure data integrity, scientific validity, and patient safety.Key...

Company Overview:Covance Latinoamérica is a leading global provider of drug development services, dedicated to improving health and advancing medical research.Position Summary:This role presents an exciting opportunity to contribute to the dynamic field of clinical research. As a Clinical Research Assistant, you will play a crucial role in supporting...

Covance Latinoamérica: Clinical Research AssistantWe are seeking a highly motivated and organized Clinical Research Assistant to join our team in Mexico. As a Clinical Research Assistant, you will play a key role in the success of our clinical trials by providing administrative support to our project team and study sites.Key Responsibilities:Act as the...

Job OverviewAs a Lead Clinical Research Associate, you will play a key role in managing local Monitors and overseeing clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, as well as data quality and study compliance on a country/regional level.Key ResponsibilitiesFacilitate regional...

{"Job OverviewAs a Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. Your primary focus will be on monitoring and site management to ensure that sites are conducting the study(ies) and reporting study data as required by the study...

Company Overview:Covance Latinoamérica is expanding its operations, providing a dynamic opportunity within a rapidly growing sector of our organization.Key Responsibilities:• Serve as the primary liaison for project teams and study sites.• Conduct Case Report Form (CRF) evaluations, generate queries, and resolve discrepancies according to established...

About the RoleCovance Latinoamérica is seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team in Mexico. As a Clinical Research Assistant, you will play a critical role in the success of our clinical trials by providing administrative support to our project teams.Key ResponsibilitiesProject Support: Act as a liaison...

About the RoleWe are seeking an experienced Clinical Research Associate to join our team as a Site Lead. As a Site Lead, you will be responsible for conducting and reporting onsite monitoring visits, as well as being involved in study startup and CRF review.This is a home-based position in Mexico, and you will be required to travel. You will be working...