Clinical Study Operations Associate

The role

You will collaborate with clinical research sites, project teams, and internal stakeholders to support the deployment of Beacon's devices in clinical studies. The role focuses on study startup, site management, and live-study monitoring.

What you will do

• Collaborate with project teams to support study startup activities.
• Act as the primary point of contact for clinical sites.
• Provide training to research sites on the use of Beacon's devices and study protocols.
• 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.
• Provide actionable feedback from research sites to inform improvements in devices and workflows.

Required qualifications

• 2-4+ years of experience in clinical project management or clinical operations roles.
• Strong organizational and project management skills.
• Excellent written and verbal communication skills in English.
• Proactive mindset with the ability to identify priorities and anticipate challenges.
• Meticulous attention to detail.
• Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.

Nice to have

• additional languages

Benefits

• equity
• PTO
• other benefits

About the company

Beacon Biosignals is transforming precision medicine for the brain, from clinical development to clinical care. They offer an at-home EEG platform for clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders.