Senior CRA
4 weeks ago
Our cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forward
We are recruiting for a Senior Clinical Research Associate / Senior Clinical Research Associate II to assist our sponsor's hematology studies.
Why IQVIA?
Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that support flexible work schedulesVariety - dynamic work environments that expose you to new experiencesCollaboration - teams that work together to achieve common goals Responsibilities 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) guidelinesWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictabilityAdminister protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issuesEvaluate 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 appropriateManage 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 phaseEnsure 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 requirementsCreate 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 documentationCollaborate and liaise with study team members for project execution support as appropriateIf applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis Requirements Experience of independent on-site monitoring in the UKYou've handled multiple protocols and sites across a variety of drug indicationsLife science degree educated or equivalent industry experienceFlexible to travel to sites as requiredThis role is not eligible for UK visa sponsorship#LIAdamThompspn 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-
Cra
2 weeks ago
Reading, United Kingdom ICON Full timeICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...
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Cra 2 and Senior Cra Roles at Iqvia Uk
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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...
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Senior Clinical Trial Assistant
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Reading, United Kingdom IQVIA Full timeOur sponsor dedicated (cFSP) team are seeking CTAs and Senior CTAs to join us on our mission to drive healthcare forward. The CTA will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist...
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Reading, United Kingdom IQVIA Full timeOur sponsor dedicated (cFSP) team are seeking CTAs and Senior CTAs to join us on our mission to drive healthcare forward. The CTA will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist...
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Reading, United Kingdom IQVIA Full timeOur cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forward! We are recruiting for a Senior Clinical Research Associate / Senior Clinical Research Associate II to assist our sponsor’s hematology studies. Why IQVIA? Growth potential - clear pathways to success for those who want to grow with us Professional...
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Reading, United Kingdom IQVIA Full timeOur cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forward! We are recruiting for a Senior Clinical Research Associate / Senior Clinical Research Associate II to assist our sponsor’s hematology studies. Why IQVIA? Growth potential - clear pathways to success for those who want to grow with us Professional...
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(Senior) Patient Recruitment Specialist
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