Clinical Trial Operations Associate
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Job Summary
To support the deployment of clinical study devices, the Clinical Trial Operations Associate will collaborate with research sites and project teams in a fully remote role, focusing on study startup, site management, and live-study monitoring while ensuring compliance with regulatory standards.
Key responsibilities
- Collaborate with project teams to support study startup activities
- Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication
- Monitor project progress, ensuring adherence to timelines, protocols, and quality standards
Required qualifications
- 2-4+ years of experience in clinical project management or clinical operations roles
- Familiarity with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong organizational and project management skills
- Proactive mindset with the ability to identify priorities and anticipate challenges
- Desire to learn more about analytics, statistics, machine learning, and clinical trials
Complete Job Description
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