Clinical Research Associate Manager

Are you passionate about clinical research and looking for a challenging role in a dynamic environment?Clinical Research Associate at ICON PlcWe are seeking a highly motivated Clinical Research Associate to join our team in Santiago, Chile. As a CRA, you will play a crucial role in identifying, selecting, initiating, and closing out investigational sites for...

Unlock a fulfilling career in clinical research with IQVIA, a global leader in advanced analytics, technology solutions and clinical research services. As a Clinical Research Associate, you will play a critical role in the planning and execution of global projects, working closely with a dynamic team of professionals.Key ResponsibilitiesPerform site...

Unlock Your Potential in Clinical ResearchAs a Clinical Research Associate at IQVIA, you'll embark on a rewarding journey that combines training, development, and mentorship to propel your career forward. Our comprehensive program ensures you're equipped to excel in this dynamic field.Key Responsibilities:Conduct site selection, initiation, monitoring, and...

Job OverviewWe are seeking an experienced Clinical Research Associate to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization.

Job Overview As a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to conduct site monitoring visits to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, and sponsor...

At ICON Plc, we're on a mission to shape the future of clinical development. As a Clinical Research Associate, you'll play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Job Description:We are seeking a skilled Clinical Research Associate...

Unlock a Career in Clinical Research with ICONWe are seeking an experienced Senior Clinical Research Associate to join our team at ICON, the world's largest and most comprehensive clinical research organization.About the RoleThis is a unique opportunity to work with a global biotechnology company that focuses on areas with unmet medical need. As a Senior...

Job SummaryWe are seeking a seasoned Clinical Research Associate to join our team at ENGINEERINGUK. In this role, you will have the opportunity to work with cutting-edge clinical research projects and contribute to the advancement of healthcare.Key ResponsibilitiesMonitoring Activities: Conduct onsite and remote monitoring activities in accordance with...

At ENGINEERINGUK, we're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join our mission to shape the future of clinical development.The RoleWe are seeking a highly skilled Study Start Up Associate II to work within a large-scale, fast-paced environment assisting the Study Start Up Team Lead in the...

Job OverviewClinical research associates play a critical role in ensuring the quality and integrity of clinical trials. As a site manager, you will be responsible for conducting monitoring visits to ensure that sites are conducting studies and reporting data as required.Essential FunctionsPerform site monitoring visits in accordance with contracted scope of...

Job OverviewAs a Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. This includes performing site monitoring visits, adapting and driving subject recruitment plans, and managing ongoing project expectations and issues.Key...

Role Overview At Engineeringuk, we're seeking a highly skilled Clinical Trial Manager to lead the planning, execution, and successful completion of clinical trials. As a key member of our research team, you will be responsible for overseeing all aspects of clinical trials, ensuring adherence to timelines, budgets, and quality standards. This critical...

Clinical Research Associate Role at ICON PlcAt ICON Plc, we are seeking a skilled Clinical Research Associate to join our dynamic team. As a Senior CRA, you will work closely with a diverse group of highly qualified professionals to ensure the success of our clinical studies.About the Role:We are looking for a talented individual with 2-3 years+ of...

Seeking a highly skilled and motivated Clinical Research Associate to join our team in Santiago, Chile. This is a remote opportunity that offers the chance to work with a world-leading healthcare intelligence and clinical research organization.About ICON plcAt ICON, we pride ourselves on fostering an inclusive environment that drives innovation and...

You will have the opportunity to work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV. You will be responsible for ensuring adherence to applicable regulations and principles of ICH-GCP.Job DescriptionAs a...

Job OverviewAs a Clinical Research Specialist at IQVIA, you will be responsible for performing tasks at a country level associated with Site Activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines. This role may also include...

**Job Title:** Clinical Research Physician - Drug Development Expert**About ICON plc:** ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome talented professionals to join us on our mission to shape the future of clinical...

Job SummaryWe are seeking a highly skilled Regulatory Submissions Coordinator to join our team in Chile. As a key member of our Regulatory Submissions department, you will play a vital role in supporting the development of safe and effective medical therapeutics.Your primary responsibilities will include:Providing day-to-day support to our Regulatory...

We are seeking a highly skilled professional to fill the role of Head of Site Management and Monitoring at MSD. This position plays a critical role in the local Global Clinical Trial Operations country management team and supports the country or cluster Clinical Research Director or Region Head in executing the Global Clinical Trial Operations strategy in...

Overview">As a Clinical Research Project Coordinator at IQVIA, you will play a crucial role in ensuring the smooth execution of site activation activities. You will serve as the single point of contact for investigative sites, managing all aspects of project planning, timelines, and regulatory documents.">Responsibilities:">">Perform site startup and...