Назад
Company hidden
10 дней назад

Manager, Clinical Study Operations

115 000 - 135 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Manager, Clinical Study Operations (Clinical Trials/MedTech): Leading clinical study operations teams and overseeing device-based trials from feasibility and site start-up through recruitment, monitoring, data collection, and close-out with an accent on process standardization, data quality, and regulatory compliance. Focus on coaching direct reports, escalating study risks, improving CTMS and SOP practices, and coordinating with sponsors, CROs, Product, Engineering, and Data Science.

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

hirify.global 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.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →