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Beacon Biosignals

Manager, Clinical Study Operations

Beacon Biosignals

. Support onboarding and ramp-up for the Clinical Study Operations team .

Posted 9/25/2026full-timeRemote • Massachusetts • United StatesMid-LevelSenior💰 $115,000 - $135,000 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Support onboarding and ramp-up for the Clinical Study Operations team
  • Translate strategic priorities into a roadmap for the area, including initiative sequencing, process investment, and team growth
  • Oversee ClinOps execution across feasibility, site start-up, enrollment, monitoring, and close-out
  • Escalate risks and blockers to leadership with clear tradeoffs and options
  • Own ClinOps KPIs and goals, track progress in Asana, and report to leadership and cross-functional partners
  • Make issue-classification and escalation decisions, including complaint versus technical-issue calls and device reconciliation/invoicing decisions
  • Lead domain-level ClinOps initiatives such as process standardization, tooling rollouts, and dashboard/reporting improvements
  • Maintain and improve ClinOps SOPs, work instructions, and CTMS practices
  • Represent ClinOps in BD conversations, feasibility discussions, and Investigator Meetings
  • Manage working relationships with sponsors and CRO intermediaries; represent Beacon directly when escalated decisions require alignment or sign-off
  • Partner with Product, Engineering, Life Science, Data Science, and BD to keep trials on track and compliant

Requirements

What you’ll need
  • 6+ years of experience in clinical trial operations in biotech, medtech, or pharma
  • Bachelor's or advanced degree in a clinical or scientific field
  • 1-2+ years directly managing people, with a track record of hiring, coaching, and performance management
  • Ability to travel up to 15% of the time for Investigator Meetings, sponsor engagements, and site visits
  • Demonstrated ownership of the clinical trial lifecycle: start-up, recruitment strategy, enrollment, monitoring, data cleaning, and close-out
  • Working knowledge of GCP, FDA and global regulatory requirements
  • Experience with SOP development and QMS practices (Qualio or similar)
  • Comfortable ramping up quickly on proprietary CTMS/eTMF tooling; prior specific-tool experience not required
  • Experience working with CROs and vendors: selection support, day-to-day oversight, and relationship management
  • Strong cross-functional communication skills
  • Comfortable operating asynchronously across time zones in a remote-first, distributed organization
  • A bias toward simplicity — able to introduce the right level of process without adding unnecessary complexity

Benefits

Comp & perks
  • Equity
  • PTO
  • Asynchronous work practices supporting a strong remote experience
  • In-person hubs in Boston, New York, and Paris
  • Remote-first, distributed organization