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8 дней назад

Senior Scientist (Biotech)

129 228 - 174 839$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Scientist (Biotech): Planning, managing, and monitoring outsourced in vivo nonclinical safety studies for innovative medicines with an accent on study design evaluation, GLP compliance, and scientific data interpretation. Focus on coordinating Study Directors and CROs, resolving complex study issues, and communicating safety results across scientific and operational teams.

Location: United States — Remote; travel of up to 30% is required for onsite study monitoring and team meetings.

Annual salary: USD 129,228.90–174,839.10 in the U.S., excluding Puerto Rico.

Company

hirify.global is a biotechnology company developing medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Plan, manage, and monitor outsourced in vivo nonclinical safety studies.
  • Serve as the primary contact for study protocols, activities, and reports, working with Study Directors and study teams.
  • Review, organize, interpret, and communicate complex nonclinical safety data and results.
  • Prepare scientific figures and presentations, write departmental guidelines and SOPs, and adapt technical information for broader audiences.
  • Facilitate meetings, report study status, and coordinate resolution plans for complex issues involving multiple parties.

Requirements

  • Master’s degree with 4 or more years of relevant nonclinical safety experience, or bachelor’s degree with 6 or more years of relevant experience.
  • Experience reviewing, analyzing, and communicating in vivo nonclinical safety data and results.
  • Experience with GLP guidelines.
  • Ability to manage multiple priorities, solve problems independently and collaboratively, and work in a fast-paced environment.
  • Ability to work remotely from the United States and travel up to 30% for onsite monitoring and meetings.

Nice to have

  • Experience as a study director, study monitor, or study coordinator for in vivo nonclinical safety studies.
  • Experience with program and study management in a scientific setting and collaboration with Contract Research Organizations.
  • Strong negotiation, influencing, communication, and change-management skills.
  • Previous people-management experience, including coaching, performance management, and staff development.
  • Proficiency with graphing software, Microsoft Office, Planisware or similar timeline management software, and Gantt charts.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus and stock-based long-term incentives.
  • Paid time off, work-life balance support, and career development opportunities.

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