Clinical Research Site Activation Specialist
7 days ago
We are seeking a highly skilled Clinical Research Site Activation Specialist to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for ensuring the successful activation of investigative sites for clinical trials.
Key Responsibilities- Serve as Single Point of Contact (SPOC) for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
- 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.
- Bachelor's Degree in a related field.
- 1 year of clinical research experience or equivalent combination of education, training, and experience.
- In-depth knowledge of clinical systems, procedures, and corporate standards.
- Strong knowledge of medical terminology and regulations.
- Broad knowledge of clinical research.
- Strong knowledge of Microsoft Office and e-mail applications.
- Effective communication, organizational, and interpersonal skills.
- Ability to work independently and to effectively prioritize tasks.
- Ability to manage multiple projects.
- Attention to detail.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
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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