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 study activities.

• Serve as the main point of contact for clinical sites.

• Provide training to research facilities on Beacon’s devices and study protocols.

• Oversee project advancement and ensure adherence to timelines, protocols, and quality benchmarks.

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

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

• Deliver 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 skills in organization and project management.

• Capability to manage multiple tasks efficiently.

• Exceptional written and verbal communication skills in English.

• Proactive attitude with the ability to identify priorities and foresee challenges.

• Keen attention to detail for precise data collection and reporting.

• Familiarity with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and clinical research regulatory standards.

• Enthusiasm for learning about analytics, statistics, machine learning, and clinical trials.

• Preference for candidates located in the Central Time Zone.

🏝️ Benefits

• Equity.

• PTO.

• Up to 5% travel requirement.

• Fully remote work.

• Asynchronous work practices.

• Access to in-person office hubs in Boston, New York, and Paris.