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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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Clinical Research Associate
2 months ago
IQVIA UK is seeking a skilled Clinical Research Associate to join our team. As a key member of our cFSP 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 integrity of study site practices.
Key Responsibilities:- Site Monitoring: Perform site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.
- Recruitment Planning: Work with sites to adapt and drive subject recruitment plans to enhance predictability.
- Protocol Training: Administer protocol and related study training to assigned sites and establish regular lines of communication.
- Quality Assurance: Evaluate the quality and integrity of study site practices and escalate quality issues as appropriate.
- Study Management: Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution.
- Documentation: Ensure copies/originals of 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.
- Communication: Collaborate and liaise with study team members for project execution support as appropriate.
- Experience: Experience of independent on-site monitoring in the UK.
- Therapeutic Areas: Monitoring experience of Oncology, Cardiovascular, Respiratory, Diabetic, Immunology, or Renal therapeutic areas.
- Education: Life science degree educated or equivalent industry experience.
- Travel: UK driving license and access to vehicle (excluding London travel zones 1 & 2) and flexibility to travel to sites as required.
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 help improve patient outcomes and population health worldwide.