Clinical Study Operations Manager
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Clinical Study Operations Manager: Managing the operational delivery of clinical studies from startup through close-out with an accent on site onboarding, protocol adherence, and regulatory compliance. Focus on driving efficient study execution, maintaining GCP standards, and acting as a primary operational partner to sponsors and research sites.
Location: Remote (US-based, preference for Central Time zone), with optional office hubs in Boston, New York, and Paris.
Salary: $90,000 – $110,000
Company
is a precision medicine company transforming brain health through an at-home EEG platform for clinical development and diagnostics.
What you will do
- Oversee study startup activities, including logistics, documentation, and data configuration.
- Serve as the primary point of contact for clinical sites to ensure smooth operations.
- Train research sites on device usage and study protocols to ensure data quality.
- Monitor project progress against timelines and regulatory standards.
- Coach peers on GCP compliance, documentation discipline, and complaint management.
- Provide actionable feedback from sites to improve internal workflows and device performance.
Requirements
- Must be based in the U.S.
- Experience in clinical project management or clinical operations.
- Strong familiarity with GCP, ICH guidelines, and clinical research regulations.
- Excellent written and verbal communication skills in English.
- Ability to manage multiple priorities in a fast-paced environment.
- Meticulous attention to detail and proactive problem-solving mindset.
Culture & Benefits
- Fully remote work environment with robust asynchronous practices.
- Access to physical office hubs in Boston, New York, and Paris.
- Comprehensive compensation package including equity and PTO.
- Culture focused on scientific impact, empathy, and diversity.
- Opportunities to learn about analytics, statistics, and machine learning.
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