Назад
Company hidden
7 дней назад

Protocol Navigator II (Clinical Research)

92 900 - 133 215$
Формат работы
hybrid
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
Protocol Navigator II (Clinical Research): Coordinating the development, review, and approval of domestic and international clinical research protocols with an accent on regulatory compliance, human subjects protection, and clinical documentation. Focus on managing concurrent protocols, coordinating IRB and scientific review submissions, interpreting regulatory requirements, and tracking timelines through study initiation and amendments.

Location: United States; currently remote with required virtual and in-person meetings at the NIH campus in Bethesda, Maryland, and potential return to office

Salary: $92,900–$133,215 per year

Company

hirify.global is a biomedical research laboratory operated by Leidos Biomedical Research, supporting cancer, infectious disease, drug development, and clinical research programs for the NIH.

What you will do

  • Provide protocol development and implementation support for domestic and international NIAID intramural research protocols.
  • Serve as the point of contact and project manager for multiple protocols in development, approval, and amendment stages.
  • Coordinate with principal investigators, medical writers, research staff, regulatory offices, IRBs, and scientific review committees.
  • Review and support the production of protocols, informed consent documents, and other study materials.
  • Prepare submissions, coordinate responses to stipulations, and track approvals required to initiate research.
  • Assess human subjects protection and regulatory issues, establish timelines, and communicate required actions and next steps.

Requirements

  • Bachelor’s degree in biomedical research, clinical trials, health, or a related field, or four years of related experience in lieu of a degree.
  • At least two years of progressively responsible biomedical research experience, including one year overseeing multiple concurrent projects or protocols.
  • Knowledge of clinical research regulations, HHS requirements, protocol and informed consent documents, and approval processes.
  • Ability to work independently and collaboratively, prioritize shifting workloads, establish timelines, track milestones, and deliver under tight deadlines.
  • Strong written and verbal communication, organizational, judgment, and relationship-building skills.
  • Proficiency in Microsoft Word, including Track Changes, and MS Office; ability to obtain and maintain a security clearance.

Nice to have

  • Experience with allergy or infectious disease research.
  • Clinical research study coordination or project management experience.
  • Registered Nurse qualification.

Culture & Benefits

  • Work supporting biomedical research and public health programs with NIH and NIAID collaborators.
  • Health and wellness programs, income protection, paid leave, and retirement benefits.
  • Remote work arrangement with potential changes to office-based work and required NIH campus meetings.
  • Work environment guided by accountability, compassion, collaboration, dedication, integrity, and versatility.

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 →