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4 дня назад

Senior Director, Clinical Research & Development

273 000 - 372 000$
Формат работы
remote (Global)
Тип работы
fulltime
Грейд
senior/director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Director, Clinical Research & Development (Clinical Development): Providing clinical evaluation for in-licensing and acquisition opportunities and supporting development of molecules emerging from discovery platforms with an accent on due diligence, clinical planning, and global regulatory strategy. Focus on leading Phase 1–2a programs, overseeing clinical execution, and evaluating drug candidates across multiple modalities and disease areas.

Location: Fully remote; can be performed from anywhere. Occasional domestic and international travel of up to 20% is expected.

Salary: $273,000–$372,000 annual.

Company

hirify.global is a global biopharmaceutical company developing treatments for patients with serious and rare diseases.

What You Will Do

  • Provide clinical input to due diligence teams assessing external molecules for potential in-licensing or acquisition.
  • Support cross-functional planning for molecules advancing from discovery platforms beyond the Late Lead Optimization stage.
  • Serve on transition teams for in-licensed, acquired, or partnered molecules as needed.
  • Oversee clinical execution, clinical development planning, and external engagement.
  • Monitor emerging science, competitive landscapes, and global standards of care across relevant disease areas.

Requirements

  • MD, MD/PhD, PharmD, or equivalent medical training.
  • At least 7 years of clinical development experience in biotech or pharmaceutical settings.
  • Meaningful drug development experience with oral small molecules and biologics; combination drug-device experience is preferred.
  • Original NDA, MAA, and J-NDA experience.
  • Experience designing, executing, and interpreting global Phase 1–2a clinical programs.
  • Strong understanding of FDA, EMA, and PMDA regulatory pathways, plus the ability to lead and influence in cross-functional matrixed organizations.

Nice to Have

  • Board certification in an internal medicine specialty.
  • Experience with combination drug-device development and later-stage programs.

Culture & Benefits

  • Medical, dental, vision, and mental health coverage, plus wellbeing reimbursement and an Employee Assistance Program.
  • Paid time off, fertility and family-forming benefits, caregiver support, and flexible work schedules.
  • 401(k) company match, annual equity awards, ESPP participation, and company-paid life and disability insurance.
  • Learning programs, LinkedIn Learning access, workshops, mentorship, and leadership development.
  • Employee resource groups, recognition programs, volunteering opportunities, and occasional in-person team collaboration.

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