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Clinical Research Specialist
2 weeks ago
About the Role
IQVIA Argentina is seeking a highly skilled Clinical Research Specialist to join our team. As a key member of our clinical operations department, you will be responsible for ensuring the quality and integrity of clinical trials conducted at sites worldwide.
Key Responsibilities
- Site Management: Perform site monitoring visits to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.
- Training and Development: Administer protocol training to assigned sites and establish regular communication channels to manage project expectations and issues.
- Quality Assurance: Evaluate the quality of study site practices and escalate quality issues as necessary.
- Project Execution: Manage the progress of assigned studies by tracking regulatory submissions, recruitment and enrollment, and data query resolution.
- Documentation: Ensure accurate and complete documentation of site management activities, monitoring visit findings, and action plans.
Requirements
- Education: Bachelor's degree in a scientific discipline or healthcare preferred.
- Experience: Minimum 4 years of on-site monitoring experience.
- Skills: In-depth knowledge of GCP and ICH guidelines, strong therapeutic and protocol knowledge, and excellent written and verbal communication skills.
- Location: Candidate must be located in-country to be considered for this role.