Clinical Study Operations Associate

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

📋 Description

• Collaborate with project teams to facilitate the initiation of studies.

• Serve as the main contact for clinical sites.

• Deliver training to research sites regarding Beacon’s devices and study protocols.

• Track project development and ensure compliance with timelines, protocols, and quality standards.

• Ensure adherence to GCP, ICH guidelines, and regulatory requirements.

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

• Offer constructive feedback from research sites to enhance devices and workflows.

⛳️ Requirements

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

• Strong organizational capabilities and project management expertise.

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

• Proactive approach with the capacity to identify priorities and foresee challenges.

• Keen attention to detail.

• Knowledge of GCP, ICH guidelines, and clinical research regulatory standards.

• Eagerness to expand knowledge in analytics, statistics, machine learning, and clinical trials.

• Must reside in the Pacific or Mountain Timezones in the U.S.

🏝️ Benefits

• Equity.

• Paid Time Off (PTO).

• Fully remote work opportunity.

• Up to 5% travel.

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

• Asynchronous work practices.