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10 часов назад

Executive Director, Clinical Research (Medical Director)

304 000 - 367 500$
Формат работы
hybrid
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
Executive Director, Clinical Research (Medical Director): Designing and overseeing early- and late-stage oncology clinical trials with an accent on medical monitoring, clinical safety and efficacy assessment, and cross-functional study execution. Focus on leading matrixed clinical teams, developing high-quality protocols, addressing Health Authority and Ethics Committee questions, and advancing novel therapies for patients.

Location: Hybrid; minimum 3 days per week onsite in either California or New Jersey, United States

Salary: $304,000–$367,500 per year, depending on skills, competency, and market demand.

Company

hirify.global is a biopharmaceutical company developing novel treatments for life-threatening diseases through a platform combining chemistry, engineering, computation, and biology.

What you will do

  • Design and conduct early- and late-stage oncology clinical development trials.
  • Assess clinical safety and efficacy data, perform medical monitoring, and oversee study-related clinical activities.
  • Lead Clinical and Clinical Study teams in a matrix environment.
  • Collaborate with biomarker, discovery, translational research, toxicology, clinical pharmacology, drug safety, regulatory, and clinical operations functions.
  • Build relationships with external investigators, key opinion leaders, and alliance partners.
  • Develop high-quality study protocols and address protocol questions from Health Authorities and Ethics Committees.

Requirements

  • MD or DO degree with 10+ years of clinical experience and significant oncology experience.
  • Significant clinical practice experience with direct patient care, preferably in oncology.
  • Proven experience leading clinical trials, including medical monitoring of early- and late-stage studies and managing complex projects.
  • In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
  • Ability to work effectively in a matrixed environment with strong analytical, organizational, problem-solving, communication, and interpersonal skills.
  • Availability for at least 3 days per week onsite in California or New Jersey, with additional onsite presence as business needs require.

Nice to have

  • Experience with IND and/or NDA filings.

Culture & Benefits

  • Bonus and equity compensation in addition to base salary.
  • 401(k) plan with company matching.
  • Medical, dental, vision, mental health, and wellness benefits.
  • Weeklong summer and winter holiday shutdowns, generous paid time off, and holiday policies.
  • Enhanced parental leave and life/AD&D insurance benefits.
  • Daily subsidized lunch when working onsite.

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