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3 дня назад

Regional Scientific Director (Gene Editing)

216 000 - 264 000$
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
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Описание вакансии

Текст:
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TL;DR
Regional Scientific Director (Gene Editing): Establishing scientific partnerships with healthcare professionals and supporting CRISPR-based gene editing programs and Phase 3 clinical trials across the Mid-Atlantic territory with an accent on scientific exchange, medical education, and clinical trial enrollment. Focus on developing KOL engagement plans, identifying site activation and recruitment barriers, and communicating complex medical evidence in a regulated environment.

Location: Home-based office, covering Maryland, Washington, D.C., Delaware, Virginia, West Virginia, North Carolina, and South Carolina; travel 50–70% with overnight stays.

Base salary: $216,000–$264,000 USD per year, plus performance-based annual bonus and equity eligibility.

Company

hirify.global develops curative CRISPR-based genome editing treatments for severe and life-threatening diseases.

What you will do

  • Build trusted scientific partnerships with KOLs, principal investigators, investigators, referral healthcare professionals, and multidisciplinary healthcare teams.
  • Provide scientific education on the CRISPR gene editing platform, mechanism of action, and clinical data for the nex-z and lonvo-z programs.
  • Develop individualized scientific engagement plans and identify external insights, knowledge gaps, and site capabilities through CRM reporting.
  • Support Phase 3 clinical trials during site start-up, activation, and recruitment by identifying barriers and discussing solutions with investigators and site teams.
  • Attend medical congresses, staff scientific booths, cover scientific sessions, gather insights, and deliver institutional presentations as appropriate.
  • Maintain scientific integrity and compliance by completing training on time and following applicable policies.

Requirements

  • Doctorate or terminal degree such as Pharm.D., Ph.D., M.D., or D.O.
  • At least 3 years of industry or related experience, including extensive Phase 3 clinical trial experience.
  • Prior pharmaceutical experience as an MSL or RSD, with strong knowledge of compliant scientific exchange and clinical trial execution.
  • Ability to communicate complex scientific and medical information effectively and deliver influential presentations to healthcare audiences.
  • Strong organization, prioritization, project management, collaboration, and cross-functional communication skills.
  • Valid driver’s license, proficiency with standard computer and video-conferencing tools, and ability to sit or stand at a computer for multiple hours.

Nice to have

  • Therapeutic knowledge in allergy, immunology, HAE, cardiology, ATTR-CM/ATTR-PN, or genetic medicine.
  • New product launch experience.

Culture & Benefits

  • Mission-driven work focused on developing potentially curative genome editing treatments.
  • Performance-based annual cash bonus.
  • New-hire equity grant and eligibility for annual equity awards.
  • Home-based work with extensive regional travel.

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