Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Очень мало
$100к-125к/год
$120к$140кмедиана$160к
По похожим ролям (50) ~ $140к/год
На СНГ рынке: $2.7к/мес ($2.1к - $4.7к)
57
Средняя вакансия
развернуть
Обязанности описаны понятно, а работа связана с клиническими исследованиями и доступна удалённо, но зарплата заметно ниже рыночного ориентира, а нагрузка включает 15–30 исследований, дежурства и частые поездки.
Кликните для подробной информации
Зарплата ниже рынкаВысокая нагрузкаЧастые поездкиПонятные обязанностиКлинические исследования
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Trials Senior Project Manager (Clinical Research): Managing global clinical trial laboratory activities from study setup through closeout with an accent on client coordination, protocol compliance, and regulatory documentation. Focus on overseeing multiple protocols, developing laboratory specifications and work instructions, coordinating regional project managers, and resolving complex study delivery issues.
Location: Remote, United States; Rochester, NY 14624. Full-time, 40 hours per week, Monday–Friday daytime schedule. The role requires overnight travel, occasional weekend travel, travel to client events and international ACM locations, and a valid passport.
Salary: $100,000–$125,000 annually
Company
hirify.global provides central laboratory services and clinical trial support.
What you will do
Act as the primary client contact for laboratory aspects of assigned clinical trials.
Manage approximately 15–30 protocols from setup through maintenance and closeout.
Coordinate regional project managers and internal functions to deliver trials according to global laboratory specifications.
Develop Global Laboratory Specification Documents, Investigator Manuals, and protocol-specific work instructions.
Lead investigator training, client meetings, quality audits, inspections, and project metric reviews.
Maintain regulatory documentation, support on-call coverage, and troubleshoot study delivery issues.
Requirements
Must be based in the United States for this remote role.
At least 3 years of project management experience.
At least 1 year of experience in clinical trials, laboratory, or healthcare settings.
Working knowledge of FDA, NYSDOH, GCP, ICH, and other relevant clinical laboratory regulations.
Ability to travel overnight, including to international locations and occasional weekend investigator meetings.
Strong problem-solving and communication skills.
Nice to have
Master’s degree.
Culture & Benefits
Remote work with a regular Monday–Friday daytime schedule.
Work involving international clinical trial programs and cross-functional collaboration.
Sedentary office-based work with reasonable accommodations available for reported physical requirements.
Potential additional pay components may apply; compensation depends on experience, qualifications, specialty, internal equity, location, and contracts.
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 →