Site Monitor

IQVIA, Inc. is expanding its Site Monitoring Expert team and seeking an experienced professional to join us. As a Site Monitoring Expert, you will perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, and evaluate the quality and integrity of study site practices.The ideal candidate will have a life science degree...

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...

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,...

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...

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...

Job Description:We are seeking a highly motivated and experienced Site Monitoring Expert to join our team. As a Site Monitoring Expert, you will be responsible for conducting site monitoring visits to ensure the integrity of clinical trials. You will work closely with sites to adapt and drive subject recruitment plans, track regulatory submissions, and...

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,...

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...

Skillful Site Monitoring Experts are required to join our team at IQVIA, working in Northern England and Scotland. This position offers an excellent opportunity to utilize your expertise in clinical research, collaborating with supportive leadership and cutting-edge technology.Job RequirementsLife science degree or equivalent industry experience6 months of...

Be Part of Our Sponsor-Dedicated Team as a Clinical Research AssociateIQVIA is seeking talented Clinical Research Associates to join our team, providing support to sites across Scotland and Northern England. This role offers a unique opportunity to work on various projects, develop your skills, and grow your career.We are looking for candidates who are...

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...

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...

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...

Clinical Research Associate - South West EnglandWe are looking for a seasoned Clinical Research Associate to join our team in the South West of England, supporting sponsors and advancing patient care.About This RoleThis position presents an exceptional opportunity for CRAs to grow professionally, leverage industry expertise, and contribute to groundbreaking...

CV-LibraryWe are seeking a highly skilled Project Monitoring Specialist to join our team. This is a great opportunity for an experienced professional to take on a challenging role and contribute to the success of our projects.The ideal candidate will have excellent project management skills, with experience in delivering complex refurbishment and fit out...

About the RoleWe have an exciting opportunity for a Traffic Marshall to work with us at Randstad Construction and Property. As a key member of our site team, you will be responsible for managing traffic flow, identifying potential hazards, and implementing effective safety protocols.Key Responsibilities:Monitor and manage traffic flow on siteConduct regular...

We are seeking highly motivated Study Site Managers to join our team at IQVIA Argentina. As a Study Site Manager, you will be responsible for overseeing the conduct of clinical trials at study sites.About the RoleEnsure compliance with regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...

Job OverviewProject People is seeking a highly skilled Site Assurance Manager to join our team. The successful candidate will lead and manage physical security and site access assurance for our passive estate.The ideal candidate will have experience in managing site-level security, digital access permit systems, and supplier delivery. They will also be...

Key ResponsibilitiesManage site operations, including staff supervision, resource allocation, and adherence to project timelines.Ensure compliance with safety regulations, conduct risk assessments, and develop method statements.Maintain accurate site diaries, monitor progress, and report to senior management.Foster a positive working environment, promoting...