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Reading, Reading, United Kingdom IQVIA Argentina Full time{"title": "Clinical Research Associate", "description": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory requirements, and collaborating with study team members to drive project execution.Key...
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Reading, Reading, United Kingdom IQVIA Argentina Full time{"title": "Clinical Research Associate", "description": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory requirements, and collaborating with study team members to drive project execution.Key...
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Reading, Reading, United Kingdom IQVIA Argentina Full time{"title": "Clinical Research Associate", "description": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for conducting site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and integrity of study site...
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Reading, Reading, United Kingdom IQVIA Argentina Full time{"title": "Clinical Research Associate", "description": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for conducting site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and integrity of study site...
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Clinical Research Associate
2 months ago
At IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials by providing administrative support to our Clinical Research Associates and Regulatory and Start-Up teams.
Key Responsibilities:- Assist Clinical Research Associates with updating and maintaining clinical documents and systems, ensuring accurate and complete Trial Master File delivery.
- Collaborate with CRAs and RSU on the preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Coordinate the tracking and management of Case Report Forms, queries, and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
- Provide training and onboarding for new Clinical Trial Assistants.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- Knowledge of applicable clinical research regulatory requirements.
- Minimum 6 months clinical research experience preferred.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Effective written and verbal communication skills, including good command of the English language.
IQVIA 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.