Clinical Study Operations Manager

14 hours, 13 minutes ago
Contract
Senior
Project and Program Management
Beacon Biosignals

Beacon Biosignals

Beacon Biosignals uses AI and EEG to transform brain disorder treatment with neurobiomarker technology, accelerating clinical trials and enhancing precision neurology.

Biotechnology
11-50
Founded 2019
$27M raised

Description

  • Collaborate with project teams to plan and launch study startup activities, including communications, logistics, documentation, and data configuration.
  • Serve as the primary operational contact for clinical sites and maintain clear communication with sponsors and internal teams.
  • Oversee site onboarding and training on Beacon devices and study protocols to support proper device use and data collection.
  • Monitor study progress and ensure adherence to timelines, protocols, quality standards, and regulatory requirements.
  • Manage study operations across startup, maintenance, and close-out phases to ensure smooth execution.
  • Maintain compliance with Good Clinical Practice (GCP), ICH guidelines, and other clinical research regulations.
  • Coach internal peers on GCP requirements, documentation discipline, version control, and complaint management.
  • Identify operational risks and escalate issues using tools such as Zendesk and Asana.
  • Collect and share site feedback to improve devices and operational workflows.

Requirements

  • 5+ years of experience in clinical project management or clinical operations roles.
  • Strong organizational and project management skills with the ability to manage multiple responsibilities.
  • Excellent written and verbal communication skills in English; additional languages are a plus.
  • Proactive mindset with the ability to identify priorities and anticipate challenges.
  • Meticulous attention to detail and accuracy in data collection and reporting.
  • Ability to work effectively in a fast-paced environment with multiple priorities.
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
  • Knowledge of decentralized data collection, compliance, and oversight.
  • Empathy for patients and clinical sites.
  • Interest in analytics, statistics, machine learning, and clinical trials.

Benefits

  • Salary range of $90,000–$110,000.
  • Equity as part of the total compensation package.
  • PTO included in the benefits package.
  • Fully remote work anywhere in the U.S.
  • Up to 10% travel.
  • Access to in-person office hubs in Boston, New York, and Paris.

Interested in this position?

Apply directly on the company website

Apply Now

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