Site Activation Manager in Clinical Research

Site Activation and Regulatory SpecialistAt IQVIA LLC, we are seeking a highly skilled Site Activation and Regulatory Specialist to join our team. In this role, you will be responsible for executing feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements.Key...

Site Activation SpecialistJob OverviewExecute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at a regional or country level.Key ResponsibilitiesPrepare and manage site documentation, reviews, and negotiations of site documents and contracts with sites and...

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 OverviewWe are seeking a highly skilled Site Activation Specialist to join our team at IQVIA Argentina. The successful candidate will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project...

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 Overview">As a Trilingual Site Activation Coordinator, you will perform tasks at a country level associated with contracts for site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. Your role may also involve...

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 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 Overview: As a Site Activation Specialist at Iqvia Argentina, you will perform critical tasks associated with site activation activities in accordance with local and international regulations, standard operating procedures, project requirements, and contractual guidelines. This role requires a professional individual contributor who works under moderate...

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...

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 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 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 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...

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 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 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 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 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...

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...