Manager Clinical Research

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, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as...

{"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...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations,Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts...

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 and adverse event reporting requirements internally and externally. Acts as primary site...

This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a particular study for...

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring activities in compliance with ICH-GCP,...

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 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 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...

At BOG Fortrea Colombia Ltda., we're seeking a talented Clinical Research Associate to contribute to our global clinical development efforts. As a leading contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development solutions across multiple therapeutic areas.Our team is...

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 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 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: 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...

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 Description This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a...

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 Description This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a...

Job SummaryBOG Fortrea Colombia Ltda. is seeking a highly skilled Sr. Payment Manager to join our team. As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.Key...