Manager, Clinical Study Operations
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Remote, with the role associated with Boston, MA. Travel up to 15% for Investigator Meetings, sponsor engagements, and site visits. Beacon supports asynchronous work across American and European time zones, with in-person hubs in Boston, New York, and Paris.
Salary: $115,000–$135,000 per year, plus equity, PTO, and other benefits.
Company
develops at-home EEG and cardiopulmonary signal platforms for clinical development and precision diagnostics in neurological, psychiatric, sleep, and central nervous system disorders.
What you will do
- Manage and coach Clinical Study Operations direct reports, supporting onboarding, performance management, and day-to-day execution.
- Oversee clinical study operations across feasibility, site start-up, recruitment, enrollment, monitoring, data collection, and close-out.
- Translate strategic priorities into roadmaps, ClinOps KPIs, process investments, and team-growth plans.
- Lead process standardization, tooling rollouts, dashboard improvements, SOP updates, and continuous process improvement.
- Represent ClinOps in business development conversations, feasibility discussions, Investigator Meetings, deal shaping, SOW input, and site planning.
- Manage sponsor and CRO relationships while partnering with Product, Engineering, Data Science, Life Science, and BD.
Requirements
- 6+ years of clinical trial operations experience in biotech, medtech, or pharma; device-based trial experience is strongly preferred.
- Bachelor’s or advanced degree in a clinical or scientific field.
- 1–2+ years of direct people-management experience, including hiring, coaching, and performance management.
- Hands-on ownership of the clinical trial lifecycle, including start-up, recruitment strategy, enrollment, monitoring, data cleaning, and close-out.
- Working knowledge of GCP, FDA and global regulatory requirements, SOP development, and QMS practices such as Qualio.
- Experience with CROs and vendors, strong cross-functional communication, and the ability to work asynchronously across time zones.
Nice to have
- Experience with device-based clinical trials.
- Experience with proprietary CTMS, eTMF, eBinder, LMS, or similar clinical operations tooling.
- Experience working in a fast-moving startup environment.
Culture & Benefits
- Remote-first and asynchronous work practices.
- Distributed Clinical Study Operations organization across American and European time zones.
- In-person hubs in Boston, New York, and Paris.
- Compensation package includes equity, PTO, and other benefits.
- Culture emphasizes curiosity, sound judgment, simplicity, self-service, empathy, and diverse teams.
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