Назад
Company hidden
7 дней назад

Sr. Director, Scientific Affairs (Clinical Research)

181 400 - 225 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
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
Sr. Director, Scientific Affairs (Clinical Research): Leading scientific affairs operations for global clinical studies, RFPs, proposals, bid defenses, and third-party laboratory relationships with an accent on protocol analysis, feasibility, budgets, and laboratory strategy. Focus on leading global laboratory networks, developing operational assay proposals, managing 3PL partnerships, and supporting complex clinical trial execution.

Location: Remote, United States. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Salary: $181,400–$225,000 USD annually, plus eligibility for a discretionary annual bonus.

Company

hirify.global provides specialty laboratory and clinical research services for biotech and pharmaceutical clients.

What you will do

  • Lead scientific affairs support for RFPs, bid defense meetings, proposals, and client pre-award discussions.
  • Analyze clinical protocols, feasibility, enrollment, timelines, assay endpoints, budgets, and operational requirements.
  • Own global third-party laboratory relationships, including capabilities, metrics, governance meetings, quotes, invoices, and billing reconciliation.
  • Develop proposal content covering assay development, validation, sample analysis, operational strategy, and clinical development planning.
  • Partner with laboratory operations, business development, proposals, vendor management, and project management teams through study start-up and delivery.
  • Represent Precision at client meetings, industry events, speaking engagements, exhibitions, and through scientific publications.

Requirements

  • Bachelor's degree in life sciences or equivalent relevant experience; an advanced degree or PhD is preferred.
  • 15+ years of experience in the CRO or laboratory industry, or equivalent relevant experience and demonstrated competencies.
  • Experience leading and influencing global laboratory networks, including multi-site operations, standardized processes, quality systems, and compliance objectives.
  • Experience with operational protocol analysis, feasibility, budget review, proposal development, and operational execution across clinical trial phases.
  • Experience managing or overseeing third-party laboratory partners.
  • Experience in relevant therapeutic-area clinical development and operational delivery strategy.

Culture & Benefits

  • Remote work within the United States.
  • Health insurance, retirement savings benefits, life insurance, and disability benefits.
  • Parental leave and paid time off for sick leave and vacation.
  • Opportunity to contribute to innovation and maintain a scientifically driven position in clinical research services.

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 →