Clinical Study Operations Associate

Beacon Biosignals

. Collaborate with project teams to support study startup activities .

Posted 10/15/2026full-timeRemote • United StatesJuniorMid-Level💰 $65,000 - $85,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical project management and operations, ensuring compliance with GCP and ICH guidelines while effectively communicating with clinical sites. Proficient in monitoring project progress and providing training on study protocols and devices.

Highest-signal resume keywords

Clinical Project ManagementGCP ComplianceICH Guidelines FamiliarityProject Management SkillsExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsStudy ProtocolsProject MonitoringRegulatory StandardsData AnalysisStatisticsMachine Learning

Soft Skills

Organizational SkillsProactive MindsetAttention to Detail

Tools & Technologies

ZendeskAsana

Industry Keywords

Clinical ResearchStudy Startup ActivitiesResearch SitesOperational Issues

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Collaborate with project teams to support study startup activities
Act as the primary point of contact for clinical sites
Provide training to research sites on Beacon’s devices and study protocols
Monitor project progress and adherence to timelines, protocols, and quality standards
Maintain compliance with GCP, ICH guidelines, and regulatory standards
Address operational issues and escalate through Zendesk and Asana
Provide actionable feedback from research sites to improve devices and workflows

Requirements

What you’ll need

2-4+ years of experience in clinical project management or clinical operations roles
Strong organizational and project management skills
Excellent written and verbal communication skills in English; additional languages are a bonus
Proactive mindset with the ability to identify priorities and anticipate challenges
Meticulous attention to detail
Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements
Desire to learn more about analytics, statistics, machine learning, and clinical trials
Must be located in the Pacific or Mountain Timezones in the U.S.

Benefits

Comp & perks

Equity
PTO
Fully remote work
Up to 5% travel
In-person office hubs available in Boston, New York, and Paris
Asynchronous work practices