Site Activation Specialist
2 semanas atrás
**Job Overview**
As a key member of our team, you will be responsible for ensuring the successful activation of investigational sites in accordance with applicable local and international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines. This role will involve collaborating with the project management team, site activation manager, and other departments to ensure adherence to quality standards and project timelines.
**Key Responsibilities**
- Under general supervision, serve as the single point of contact for investigative sites, site activation manager, and project management team.
- Perform start-up and site activation activities according to applicable regulations, SOPs, and work instructions.
- Prepare site regulatory documents, reviewing for completeness and accuracy.
- Ensure accurate completion and maintenance of internal systems, databases, and tracking tools with project-specific information.
- Review and provide feedback to management on site performance metrics.
- Review, establish, and agree on project planning and project timelines.
- Provide local expertise to site activation managers and project teams during initial and ongoing project timeline planning.
**Requirements**
1 year of clinical research experience, or an equivalent combination of education, training, and experience. IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
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