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Associate Director, Office for Human Research Studies

106 400 - 118 000$
Формат работы
hybrid
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
Associate Director, Office for Human Research Studies (IRB and Clinical Research Compliance): Overseeing scientific and IRB review of cancer-related human subject research across the Harvard Cancer Consortium with an accent on regulatory compliance, HIPAA oversight, and single IRB coordination. Focus on managing complex reliance agreements, educating IRB staff and members, supervising analysts, and ensuring consistent operations across seven IRB committees.

Location: Fully remote from a New England state only (ME, VT, NH, MA, CT, or RI), with occasional onsite work as needed; office address in Brookline, Massachusetts.

Salary: $106,400–$118,000 per year.

Company

hirify.global conducts cancer research, provides patient care, educates physician-researchers, and collaborates with Harvard-affiliated hospitals.

What you will do

  • Oversee the review and approval of clinical and non-clinical research across the Harvard Cancer Consortium.
  • Serve on seven IRB committees and ensure determinations comply with human subject protection regulations and HIPAA.
  • Lead single IRB reliance agreements, including local context collection, external IRB communication, and outcome coordination.
  • Create and deliver education programs for IRB members and OHRS staff, including certified IRB professional training.
  • Supervise Senior IRB Analysts, protocol-focused IRB Analysts, and Meeting Coordinators.
  • Maintain IRB policies and procedures, report non-compliance and research problems to oversight agencies, and improve operational consistency across committees.

Requirements

  • Bachelor’s degree.
  • At least five years of experience in a cancer center and/or with an academic IRB or research office.
  • At least three years of staff management experience.
  • Expertise applying federal regulations to clinical research and knowledge of HIPAA requirements for research.
  • Strong written and verbal communication, analytical, problem-solving, and decision-making skills.
  • Ability to work remotely only from ME, VT, NH, MA, CT, or RI and attend onsite activities when required.

Nice to have

  • CIP certification.

Culture & Benefits

  • Remote work arrangement with occasional onsite participation.
  • Work within a collaborative Harvard Cancer Consortium research environment.
  • Focus on inclusive, diverse, equitable, and compassionate patient care and research.
  • Opportunity to represent OHRS at professional conferences and external meetings.

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