Clinical Study Operations Associate
New
B
Beacon BiosignalsBiotechnology
Fully remote anywhere in the U.S., Central Time Zone preferredFull-TimeMiddle
Salary$65,000 – $85,000
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Job Details
- Languages
- English
- Experience
- 2-4+ years
- Required Skills
- Project ManagementGCPAsanaZendesk
Requirements
- 2-4+ years of experience in clinical project management or clinical operations roles.
- Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively.
- Excellent written and verbal communication skills in English.
- Proactive mindset with the ability to identify priorities and anticipate challenges.
- Meticulous attention to detail, ensuring accuracy in data collection and reporting.
- Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
- Desire to learn more about analytics, statistics, machine learning, and clinical trials.
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.
- Provide training to research sites on the use of Beacon’s devices and study protocols, ensuring proper device usage and data collection.
- Monitor project progress, ensuring adherence to timelines, protocols, and quality standards.
- Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards.
- Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution.
- Provide actionable feedback from research sites to inform improvements in devices and workflows.
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