Clinical Study Operations Associate

Beacon Biosignals

. Collaborate with project teams to support study startup activities .

Posted 9/23/2026full-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 utilizing project management tools to monitor progress and enhance workflows.

Highest-signal resume keywords

Clinical Project ManagementGCP ComplianceICH Guidelines FamiliarityProject Management SkillsCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical OperationsStudy ProtocolsRegulatory StandardsData AnalysisStatisticsMachine LearningAttention to Detail

Soft Skills

Organizational SkillsProactive MindsetProblem-Solving Skills

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 tools such as 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 based in the Pacific or Mountain Timezones in the U.S.

Benefits

Comp & perks

Equity
PTO
Up to 5% travel
Fully remote work with asynchronous work practices
Access to in-person office hubs in Boston, New York, and Paris