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...

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...

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...

Job DescriptionThis 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.Key Responsibilities:Main Point of Contact (POC)...

Job DescriptionThis 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...

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,...

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 DescriptionThis role is a key position within MSD, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. We value diversity and inclusivity in all aspects of our organization.The primary responsibility of this Clinical Research Manager is to oversee the end-to-end performance and project...

About the Role:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will play a vital role in ensuring the successful delivery of clinical trials.Job Summary:The Clinical Research Associate will be responsible for coordinating and conducting site...

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 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...

Clinical Research Associate Job Summary:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. This role 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 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...

Company OverviewIqvia Argentina is a leading healthcare consulting firm that helps clients navigate the complexities of clinical research. We are seeking a highly skilled and experienced Site Activation Manager to join our team.Salary$65,000 - $80,000 per annum, depending on experience.Job DescriptionWe are looking for a talented Site Activation Manager to...

Job DescriptionThis 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.Key Responsibilities:Act as the main point of...