Regulatory Affairs Associate
5 days ago
Job Summary
We are seeking a highly motivated and detail-oriented Site Activation Coordinator to join our team at IQVIA Argentina.
Key Accountabilities
- Review documents for completeness, consistency, and accuracy under the guidance of senior staff, along with preparing site regulatory documents and reviewing them for completeness and accuracy.
- Track and follow up on the progress, approval, and execution of documents, including regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, and distribute completed documents to sites and internal project team members.
- Support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
Requirements
- Bachelor's Degree in Life Science or related field preferred
- Minimum 2 years' work experience; 1+ years in healthcare or similar
- Good interpersonal, communication, and organizational skills to establish and maintain effective working relationships with co-workers, managers, and sponsors
- Ability to work on multiple projects
Why Join Us
- Exposure across 21 Therapeutic Areas
- Be part of a global team operating across 141 locations
- Exposure across a variety of studies and projects
- Access to new, innovative technologies
- Work within a collaborative and vibrant environment
- Own your career
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