Clinical Research Site Coordinator

At PSI CRO, we are seeking a highly skilled Clinical Research Coordinator to join our international team. As a key support to clinical research projects, you will be responsible for streamlining communication, maintaining systems, and managing documents & information.Responsibilities:Act as the main point of contact between site personnel and CRA involved in...

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...

About the RoleMERCK GRUPPE - MSD SHARP & DOHME is seeking a highly skilled Clinical Research Associate - Site Manager to join our team. In this role, you will be responsible for managing clinical research sites and ensuring the successful execution of our studies.Key ResponsibilitiesManage clinical research sites and ensure compliance with regulations and...

Job Title:Clinical Research AssociateJob Summary:We are seeking a highly motivated and experienced Clinical Research Associate to join our team at MSD. The successful candidate will be responsible for managing and monitoring clinical trials at various research sites.Key Responsibilities:Manage and monitor clinical trials at research sitesConduct site...

Job DescriptionThe Clinical Research Associate will be responsible for ensuring the compliance of study conduct with ICH/GCP and country regulations, Company policies and procedures, quality standards, and adverse event reporting requirements internally and externally.Key Responsibilities:Develop and maintain strong site relationships and ensure continuity...

Job DescriptionThe Clinical Research Associate (CRA) is accountable for ensuring the performance and compliance of assigned protocols and sites in a country. Under the oversight of the CRA manager, the CRA ensures compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards, and adverse event reporting requirements...

Job Title: Senior Clinical Research AssociateJob Summary:The Senior Clinical Research Associate will be responsible for managing and monitoring clinical research studies in a country, ensuring compliance with ICH/GCP and country regulations. The role will involve developing and expanding the territory for clinical research, finding and developing new sites,...

We are seeking a skilled Clinical Trial Administrator to assist with the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.Support the preparation of study-related...

Job Title: Clinical Operations CoordinatorJob Summary:We are seeking a highly skilled Clinical Operations Coordinator to join our team at ENGINEERINGUK. As a Clinical Operations Coordinator, you will play a critical role in supporting the regional leadership governance meetings and actions, capabilities & country input for sales/PM/Feasibility/SSU, etc.Key...

Job Description:The Clinical Research Associate will be responsible for ensuring compliance with ICH/GCP and country regulations. The candidate will have strong site relationships and ensure continuity throughout all phases of the trial.Responsibilities:Develops strong site relationships and ensures continuity of site relationships.Performs clinical study...

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:At PSI CRO, we are seeking a highly skilled and experienced Clinical Research Associate to join our international team. As a key member of our team, you will play a crucial role in supporting clinical research projects by streamlining communication, maintaining systems, and managing documents and information.Key Responsibilities:Be the main...

Job SummaryWe are seeking a highly skilled Clinical Research Associate (CRA) to join our team at MSD. As a CRA, you will be responsible for ensuring the successful execution of clinical trials at assigned sites. This is a fantastic opportunity to work in a dynamic and collaborative environment where you will have the chance to develop your skills and...

Job Summary: We are seeking a highly organized and detail-oriented Clinical Research Associate to join our team at PSI CRO. As a Clinical Research Associate, you will play a critical role in the success of our clinical research projects. Your primary responsibility will be to serve as the main point of contact between site personnel and CRA involved in the...

Job Title: Site Management Associate IJob Summary: We are seeking a highly organized and detail-oriented Site Management Associate I to join our team at PSI CRO. As a Site Management Associate I, you will be responsible for ensuring the smooth operation of clinical research projects at our sites.Key Responsibilities:Site Management: Serve as the primary...

Job DescriptionThe role of Senior Clinical Research Associate 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, and adverse event reporting...

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...

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 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...

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...