Study Site Manager

About the RoleThis Study Start Up Associate II position is an integral part of our team, ensuring that study sites are ready to start clinical trials. You will work closely with study sites, sponsors, and internal personnel to negotiate CTAs, budgets, and ancillary agreements.ResponsibilitiesNegotiate contracts and budgets with study sites.Oversee...

About the Opportunity:We are seeking a Site Management Specialist to join our team at IQVIA UK. As a Site Management Specialist, you will be responsible for managing the progress of assigned studies, tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and...

Pharmiweb is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.About the...

Home based in the United Kingdom, we are seeking a highly skilled Senior Toxicology Study Manager to partner with our global pharmaceutical client. This is an exciting opportunity for you to join their team and contribute to the development of innovative medicines.About the RoleIn this fully home-based position, you will be responsible for leading study...

Job Overview:We are seeking a highly skilled Clinical Research Associate to join our team in the South West of England. As a Clinical Research Associate, you will be responsible for performing site monitoring visits in accordance with contracted scope of work and regulatory requirements.You will work with sites to adapt, drive, and track subject recruitment...

About the RoleWe are looking for an experienced Clinical Research Associate to join our team at IQVIA, Inc.The ideal candidate will have a strong background in clinical research and excellent communication skills.Responsibilities:Conduct site monitoring visits to ensure compliance with regulatory requirements.Collaborate with sites to develop and implement...

About the JobIn this role, you will work with sites to adapt, drive, and track subject recruitment plans, and manage the progress of assigned studies by tracking regulatory submissions and approvals. You will also ensure that site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is...

About the RoleWe are looking for a skilled Clinical Research Associate to join our sponsor-dedicated team in the South West of England.As a Clinical Research Associate, you will be responsible for performing site monitoring visits and ensuring the quality and integrity of study site practices.You will work closely with sites to adapt and track subject...

As a Clinical Research Associate at ICON plc, you will play a key role in the success of our clinical trials.This is an exciting opportunity to work with a world-leading healthcare intelligence and clinical research organization, based in the UK.About the Role:As a Clinical Research Associate, you will be responsible for coordinating clinical trial...

Job DescriptionThis Study Start-Up Associate Manager position plays a vital role in the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.You will be responsible for managing and maintaining comprehensive and accurate records of regulatory submissions,...

Clinical Research Associate Job SummaryAbout UsENGINEERINGUK is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.Job ResponsibilitiesWe are seeking a Clinical Research Associate to join our team in the UK. The successful candidate will be responsible...

Seeking a talented Clinical Research Associate to support our team in the South West of England. This role offers an exciting opportunity for CRAs who value supportive leadership, collaborative teams, and technology-enabled resources.The successful candidate will be responsible for conducting site monitoring visits, adapting subject recruitment plans,...

Pharmiweb Career OpportunityWe are seeking an experienced Clinical Research Associate to join our dynamic team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in ensuring the successful execution of clinical trials by conducting site monitoring visits, adapting subject recruitment plans, and evaluating study site practices.To...

Lead Your Career with Study International">We are a leading organization in the field of software development, committed to innovation and excellence.We are seeking a talented Lead Software Engineer to join our team in Reading.This role involves designing, developing, and maintaining cutting-edge software solutions using modern technologies to deliver...

Clinical Research AssociateWe are seeking a Clinical Research Associate to join our sponsor-dedicated team and support sites across Northern England and Scotland.This is an excellent opportunity for CRAs local to Northern England or Scotland who would value:Supportive leadership and collaborative teamsA variety of career opportunities to allow you to grow as...

We are seeking a Site Monitoring Expert to join our team in the South West of England. In this role, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and evaluating the quality and integrity of study site practices.About IQVIAIQVIA is a leading global provider of clinical research services,...

We are seeking a talented Site Monitoring Specialist to join our team in Northern England and Scotland. As a key member of our sponsor-dedicated team, you will play a crucial role in supporting sites across the region.Job SummaryAs a Site Monitoring Specialist, you will be responsible for performing site initiation, monitoring, and close-out visits, adapting...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.About the RoleWe are looking for a skilled Clinical Research Associate to join our team in Argentina. As a CRA, you will be responsible for conducting site monitoring visits, administering protocol and related...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.Salary & BenefitsWe offer competitive salaries with a range of $80,000 - $110,000 per year, depending on experience. Our comprehensive benefits package includes health insurance, retirement savings plan, paid...

Job OverviewWe are seeking an experienced Site Monitoring Specialist to join our cFSP (sponsor-dedicated) team at IQVIA UK. The successful candidate will be responsible for performing site monitoring visits and ensuring the quality and integrity of study site practices.About Our CompanyIQVIA is a leading global provider of clinical research services,...