Cra 2 (Clinical Research Associate), Argentina, Iqvia Biotech

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IQVIA Biotech is hiring in Argentina! Join our team as a Clinical Research Associate.
The ideal candidate will have varied therapeutic experience and be willing to work across multiple therapeutics including Oncology, Cardiovascular, Internal Medicine, & Ophthalmology.
This role is home-based in Buenos Aires, Argentina.

Job Description Summary Perform monitoring and site management work to ensure sites are conducting the study(ies) and reporting data as required by the study protocol, regulations, guidelines, and sponsor requirements.

Essential Functions Perform site monitoring visits (selection, initiation, monitoring, and close-out) in accordance with scope of work and regulatory requirements, i.e., GCP and ICH guidelines. Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability. Administer protocol and study training to sites and establish communication to manage expectations and issues. Evaluate the quality of site practices related to protocol conduct and compliance; escalate issues as needed. Manage study progress by tracking regulatory submissions, recruitment, CRF completion, data queries, and support start-up if applicable. Ensure site documents are properly filed in the TMF and ISF maintained per GCP and local regulations. Create and maintain documentation of site management, visit findings, and action plans, including reports and follow-up letters. Collaborate with study team members for project support. Support development of site-specific recruitment plans and manage site financials if applicable. Qualifications Bachelor's Degree in a scientific or healthcare field preferred.
Req. At least 1 year of on-site monitoring experience.
Req. Equivalent education, training, and experience may be accepted.
Req. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence.
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