Clinical Research Site Coordinator

Clinical Research Opportunities at PSI CRO **Job Summary** We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at PSI CRO. As a Clinical Research Coordinator, you will play a critical role in supporting clinical research projects, ensuring seamless communication, and maintaining accurate records. **Key...

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 DescriptionSeeking a highly organized and detail-oriented Clinical Research Coordinator to join our international team at PSI CRO. As a key support to clinical research projects, you will be responsible for streamlining communication, maintaining systems, and managing documents and information.Key Responsibilities:Act as the primary point of contact...

Job DescriptionAs a key member of our international team, you will play a crucial role in supporting clinical research projects by streamlining communication, maintaining systems, and managing documents and information.We are seeking a highly organized and detail-oriented individual to join our team as a Site Management Associate I. The successful candidate...

Job DescriptionAs a key member of our international team, you will play a crucial role in supporting clinical research projects by streamlining communication, maintaining systems, and managing documents and information.We are looking for a highly organized and detail-oriented individual who can work effectively in a dynamic team environment.Key...

Clinical Trial Coordinator **Job Summary** We are seeking a highly motivated and organized Clinical Trial Coordinator to join our team at CDS Fortrea Inc. As a Clinical Trial Coordinator, you will be responsible for coordinating clinical trials, managing site performance, and ensuring compliance with study protocols. **Responsibilities** * Serve as the...

Job Title: Sr Clinical Trial CoordinatorFortrea is seeking a highly motivated and organized Sr Clinical Trial Coordinator to join our team. As a key member of our clinical operations team, you will be responsible for coordinating and managing clinical trials from start to finish.Responsibilities:Coordinate and manage site contacts, including creating contact...

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,...

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 Title: Sr Clinical Trial CoordinatorAt CDS Fortrea Inc., we are seeking a highly motivated and detail-oriented Sr Clinical Trial Coordinator to join our team. As a key member of our clinical operations team, you will be responsible for coordinating and managing clinical trials from start to finish.Responsibilities:Serve as the primary point of contact...

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 Title: Sr Clinical Trial CoordinatorCDS Fortrea Inc. is seeking a highly motivated and detail-oriented Sr Clinical Trial Coordinator to join our team. As a key member of our clinical operations team, you will be responsible for coordinating and managing clinical trials from start to finish.Responsibilities:Serve as the primary point of contact for...

Job Title: Sr Clinical Trial CoordinatorCDS Fortrea Inc. is seeking a highly motivated and detail-oriented Sr Clinical Trial Coordinator to join our team. As a key member of our clinical operations team, you will be responsible for coordinating and managing clinical trials from start to finish.Responsibilities:Serve as the primary point of contact for...

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...

{"title": "Clinical Research Associate", "content": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for coordinating all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, and...

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 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 OverviewAs a Clinical Research Associate Lead at PSI, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to manage local Monitors, supervising clinical monitoring and site management activities to verify the protection of trial subjects' rights, safety, and well-being, data quality, and study...