Clinical Research Associate

{"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 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 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 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 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 Summary:We 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 monitoring investigator sites to ensure the accuracy and validity of CRF entries in relation to patient records/clinic notes (source document verification). You will also assess...

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 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...

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...

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...

About BOG Fortrea Colombia Ltda.We are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Our team of experts provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across...

Job Title: Lead CRAJob Summary:We are seeking a highly skilled and experienced Lead Clinical Research Associate to join our team at PSI. As a Lead CRA, you will be responsible for managing local monitors, supervising clinical monitoring and site management activities, and ensuring the protection of trial subjects' rights, safety, and well-being.Key...

About BOG Fortrea Colombia Ltda.We are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.Our MissionWe provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20...

About BOG Fortrea Colombia Ltda.We are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.Our MissionWe provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20...

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...

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 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 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: Clinical Research Site CoordinatorJob Summary: We are seeking a highly organized and detail-oriented Clinical Research Site Coordinator to join our team at PSI CRO. The successful candidate will be responsible for coordinating clinical research projects, ensuring compliance with regulatory requirements, and providing excellent support to site...

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...