Clinical Study Operations Associate

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

📋 Description

• Collaborate with project teams to facilitate the initiation of study activities.

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

• Deliver training to research sites regarding the use of Beacon’s devices and study protocols, ensuring proper device utilization and accurate data collection.

• Oversee project progression, guaranteeing compliance with timelines, protocols, and quality standards.

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

• Quickly address operational challenges, utilizing tools like Zendesk and Asana for resolution.

• Offer constructive feedback from research sites to guide enhancements in devices and workflows.

⛳️ Requirements

• Background in clinical project management or clinical operations roles.

• Strong organizational and project management abilities, capable of handling multiple responsibilities efficiently.

• Exceptional written and verbal communication skills in English; knowledge of additional languages is an advantage.

• A proactive approach with the capability to identify priorities and foresee potential challenges.

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

• Understanding of GCP, ICH guidelines, and clinical research regulatory mandates.

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

🏝️ Benefits

• Beacon's comprehensive asynchronous work practices provide a premium remote work experience.

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