Clinical Research Associate

At ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical research. We're seeking a Senior Clinical Research Associate to join our dynamic team and contribute to the advancement of innovative treatments and therapies.Key Responsibilities:Conduct site qualification, initiation, monitoring, and...

Clinical Research Associate - UK, ReadingICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department,...

At ENGINEERINGUK, we're seeking a skilled Clinical Research Associate to join our team in the UK. As an IHCRA, you'll play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesAssist in the planning, initiation, and execution of clinical trial...

At ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a talented Clinical Research Associate to join our diverse and dynamic team.About the RoleAs a Clinical Research Associate at ICON, you'll play a pivotal role in supporting the execution and management of clinical trials. Your contributions...

Clinical Research Associate - UKICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical Research Associate to join our...

Job SummaryClinical Research Associate - Site Monitoring ExpertIQVIA Argentina is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory requirements, and collaborating with study team members to execute...

Job SummaryPharmiweb is seeking an experienced Clinical Research Associate to join our team in the UK. As a Clinical Research Associate, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and administering protocol and related study training to assigned sites.Key...

Job SummaryPharmiweb is seeking an experienced Clinical Research Associate to join our team in the UK. As a Clinical Research Associate, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and managing the progress of assigned studies.Key ResponsibilitiesPerform site monitoring...

Job Summary:IQVIA UK is seeking an experienced Clinical Research Associate (CRA) to strengthen our cFSP team. As a CRA, you will perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, and administer protocol and related study training.Key Responsibilities:Perform site monitoring visits (selection, initiation,...

Role OverviewAs a Clinical Research Associate - Sponsor Dedicated, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and administering protocol and related study training.Key ResponsibilitiesPerform site monitoring visits in accordance with contracted scope of work and regulatory...

Job Overview:As a Clinical Trials Assistant, you will play a vital role in ensuring the successful execution of clinical trials. You will be responsible for providing administrative support to the clinical team, ensuring that all clinical documents and systems are accurately updated and maintained. This position requires strong organizational skills and...

Key Responsibilities:As a Clinical Research Associate - Site Monitoring Specialist, you will be responsible for performing site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. You will work with sites to adapt, drive, and track subject recruitment plans to enhance...

Job SummaryWe are seeking a skilled Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and administering protocol and related study training to assigned sites.Key ResponsibilitiesPerform...

Job SummaryAs a Clinical Research Associate - Sponsor Dedicated, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and evaluating the quality and integrity of study site practices. You will also manage the progress of assigned studies, track regulatory submissions and approvals,...

About the RoleWe are seeking an experienced Clinical Research Associate to join our Sponsor Dedicated team. As a CRA, you will be responsible for performing site monitoring visits, working with sites to adapt and track subject recruitment plans, and administering protocol and related study training.Key ResponsibilitiesPerform site monitoring visits to ensure...

Role OverviewWe are seeking an experienced Clinical Research Associate to join our Sponsor Dedicated team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and administering protocol and related study training.Key ResponsibilitiesPerform site...

Job SummaryIQVIA UK is seeking an experienced Clinical Research Associate to strengthen our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and ensuring the quality and integrity of study site practices.Key ResponsibilitiesPerform site monitoring visits in...

Job Summary:Pharmiweb is seeking an experienced Clinical Research Associate to strengthen our team. As a key member of our clinical operations team, you will be responsible for performing site monitoring visits, collaborating with sites to adapt and drive subject recruitment plans, and ensuring the quality and integrity of study site...

Job SummaryWe are seeking a highly experienced Clinical Research Associate to join our team in the UK. As a CRA, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and ensuring the quality and integrity of study site practices.Key ResponsibilitiesPerform site monitoring visits in accordance with...

Job SummaryWe are seeking a skilled Clinical Research Associate to join our team in the UK. As a CRA, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and evaluating the quality and integrity of study site practices.Key ResponsibilitiesPerform site monitoring visits in accordance...