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2 дня назад

Senior Director, Clinical Research (Medical Director) (Oncology)

270 000 - 325 500$
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
Senior Director, Clinical Research (Medical Director) (Oncology): Designing and conducting early-stage clinical development trials while providing medical leadership, safety and efficacy assessment, and operational oversight with an accent on oncology drug development, medical monitoring, and regulatory compliance. Focus on interpreting clinical data, coordinating cross-functional study execution, and addressing protocol questions from Health Authorities and Ethics Committees.

Location: Jersey City, New Jersey, United States; minimum 3 days per week onsite in the New Jersey office

Salary: $270,000–$325,500 per year, depending on skills, competency, and market demand

Company

hirify.global Therapeutics is a biopharmaceutical company developing treatments for life-threatening diseases through a platform combining chemistry, engineering, computation, biology, and molecular-resolution live-cell imaging.

What you will do

  • Serve as Study Responsible Physician and provide medical leadership and operational oversight for clinical development studies.
  • Design and conduct early-stage oncology and/or non-oncology clinical trials.
  • Assess clinical safety and efficacy data, perform medical monitoring, and oversee study-related clinical activities.
  • Interpret research reports and prepare oral and written product research results.
  • Coordinate with discovery, translational and biomarker research, toxicology, clinical pharmacology, drug safety, regulatory, clinical science, data management, clinical operations, and biostatistics functions.
  • Address protocol questions from Health Authorities and Ethics Committees.

Requirements

  • MD or DO degree with significant oncology experience.
  • 5–7 years of clinical experience, including 3 or more years in drug development.
  • Clinical practice experience with direct patient care.
  • Proven experience leading clinical trials and performing medical monitoring across early- and late-stage studies.
  • In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
  • Strong analytical, organizational, problem-solving, communication, and cross-functional collaboration skills.

Nice to have

  • Experience with IND and/or NDA/BLA filings.

Culture & Benefits

  • Collaborative, matrixed environment involving cross-functional development and clinical study teams.
  • 401(k) plan with company matching.
  • Medical, dental, and vision insurance with substantial company premium coverage.
  • Mental health and wellness benefits, enhanced parental leave, and generous paid time off and holiday policies.
  • Weeklong summer and winter holiday shutdowns.
  • Subsidized daily lunch when working onsite, plus life and AD&D insurance.

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