Clinical Study Operations Associate

📋 Description

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

• Serve as the main contact for clinical sites, guaranteeing efficient operations and effective communication.

• Train research sites on the operation of Beacon’s devices and study protocols, ensuring correct device application and data gathering.

• Oversee project development, ensuring compliance with timelines, protocols, and quality benchmarks.

• Ensure adherence to Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory requirements.

• Tackle operational challenges swiftly, utilizing tools like Zendesk and Asana for resolution.

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

⛳️ Requirements

• Background in clinical project management or clinical operations positions.

• Strong organizational and project management capabilities, with the ability to juggle multiple responsibilities effectively.

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

• A proactive approach with the capacity to discern priorities and foresee challenges.

• Keen attention to detail, ensuring precision in data collection and reporting.

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

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

🏝️ Benefits

• Beacon's comprehensive asynchronous work practices provide a top-notch remote work environment.

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