Clinical Study Operations Associate

This is a fully remote position, open to applicants in United States.

📋 Description

• Collaborate with project teams to facilitate study startup activities.

• Serve as the primary liaison for clinical sites.

• Provide training for research sites on Beacon’s devices and study protocols.

• Oversee project progress, ensuring adherence to timelines, protocols, and quality standards.

• Ensure compliance with GCP, ICH guidelines, and regulatory standards.

• Address operational challenges and escalate issues via Zendesk and Asana.

• Offer actionable insights from research sites to enhance devices and workflows.

⛳️ Requirements

• 2-4+ years of experience in clinical project management or clinical operations roles.

• Strong organizational and project management capabilities.

• Exceptional written and verbal communication skills in English; proficiency in additional languages is a plus.

• A proactive mindset with the capacity to identify priorities and foresee challenges.

• Keen attention to detail.

• Familiarity with GCP, ICH guidelines, and regulatory requirements in clinical research.

• A strong desire to expand knowledge in analytics, statistics, machine learning, and clinical trials.

🏝️ Benefits

• Equity.

• PTO.

• Remote work with asynchronous work practices.

• Up to 5% travel.

• In-person office hubs located in Boston, New York, and Paris.