Current jobs related to Senior CRA - Reading - IQVIA
-
Cra 2 and Senior Cra Roles at Iqvia Uk
3 months ago
Reading, United Kingdom Novasyte Full timeCRA 2 and Senior CRA roles at IQVIA UK About Us IQVIA is the largest provider of biopharmaceutical development and commercial outsourcing services and a global leader in healthcare intelligence. With a global team of 67,000+ working across 100 countries, we harness insights, commercial and scientific depth, and executional expertise to empower clients to...
-
Senior Clinical Trial Assistant
4 months ago
Reading, United Kingdom Novasyte Full timeDo you want to grow your career with the World’s largest CRO? Our Sponsor Dedicated team are recruiting for a Senior Clinical Trial Assistant to join us on our mission to drive healthcare forward. IQVIA offer genuine career progression (named on LinkedIn’s Top Companies: The 25 best workplaces to grow your career in the UK), supportive leadership, team...
-
Clinical Research Associate
12 hours ago
Reading, Reading, United Kingdom IQVIA, Inc. Full timeSenior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...
-
Clinical Research Associate
16 hours ago
Reading, Reading, United Kingdom IQVIA, Inc. Full timeSenior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...
-
Senior Clinical Research Associate II
7 days ago
Reading, United Kingdom Pharmiweb Full timeIQVIA UK are seeking Senior Clinical Research Associates (SR CRA II) to strengthen our cFSP team (sponsor-dedicated).ResponsibilitiesPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on...
-
(Senior) Patient Recruitment Specialist
4 months ago
Reading, United Kingdom Novasyte Full timeWe have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment/engagement, to join our Site and Patient Networks team. PURPOSE Assist Patient Recruitment Leads and manage assigned tasks related to the coordination, planning, and implementation of Patient Recruitment and Retention...
-
Project Manager
4 days ago
Reading, United Kingdom Morson Talent Full timeProject Controller Job DescriptionMorson Talent is partnering with a leading client in the Reading area to recruit a Project Controller.Job Title: Project ControllerSite Location: ReadingHybrid working.Duration: 5 YearsRates: £500 per dayThe primary purpose of this role is to ensure that best practice Project Controls are deployed across the project with a...
-
Project Manager
5 days ago
Reading, United Kingdom Morson Talent Full timeProject Controller Job DescriptionMorson Talent is partnering with a leading client in the Reading area to recruit a Project Controller.Job Title: Project ControllerSite Location: ReadingHybrid working.Duration: 5 YearsRates: £500 per dayThe primary purpose of this role is to ensure that best practice Project Controls are deployed across the project with a...
Senior CRA
3 months ago
Our cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forward
We are recruiting for multiple Senior Clinical Research Associates / Senior Clinical Research Associate IIs, open to candidate across the UK, remote working with travel to sites.
Why IQVIA?
Growth potential - clear pathways to success for those who want to grow with us Professional development - resources that promote your career growth and programs to help you build knowledge and gain skills Work-life balance - leaders that support flexible work schedules Variety - dynamic work environments that expose you to new experiences Collaboration - teams that work together to achieve common goalsResponsibilities
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team members for project execution support as appropriate If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basisRequirements
Experience of independent on-site monitoring in the UK You've handled multiple protocols and sites across a variety of drug indications Life science degree educated or equivalent industry experience Flexible to travel to sites as requiredThis role is not eligible for UK visa sponsorship
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
