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Irb Director Jobs (NOW HIRING)

StartCare

Director of Research

Brooklyn, NY · On-site

The Director will ensure all procedures are conducted in compliance with internal and external IRB requirements for the ethical conduct of research, as well as with HIPAA and CFR standards for ...

Sysmex

Director, Clinical Affairs

Mundelein, IL · On-site

$81K - $111K/yr

... IRB-approved studies conducted in the RACA Laboratory. The Director will also be responsible for ... maintaining relationships with outside institutions required to conduct the evaluations. Essential ...

Womans

Scientific Research Director

Baton Rouge, LA · On-site

$102.13 - $151.92/hr

Description Woman's Hosp Main Campus 100 Woman's Way Baton Rouge, LA 70817, USA The Director of ... Drafts, revises, and submits regulatory material to IRB and R&D; processes and executes IRB ...

Sysmex

Director, Clinical Affairs

Lincolnshire, IL · On-site

$84K - $114K/yr

... IRB-approved studies conducted in the RACA Laboratory. The Director will also be responsible for ... maintaining relationships with outside institutions required to conduct the evaluations. Essential ...

Sysmex

Director, Clinical Affairs

Lincolnshire, IL

$84K - $114K/yr

... IRB-approved studies conducted in the RACA Laboratory. The Director will also be responsible for ... maintaining relationships with outside institutions required to conduct the evaluations. Essential ...

HiredFirst

Director of Cardiac Care

Panama, FL · On-site

$105K - $125K/yr

The Director evaluates and recommends new technologies and services, develops comprehensive education programs for both staff and patients, and leads IRB research projects. Additional ...

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How much do irb director jobs pay per year?

As of Aug 21, 2026, the average yearly pay for irb director in the United States is $90,903.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,000.00 and $119,000.00 per year, depending on experience, location, and employer.

What is an IRB director?

An IRB (Institutional Review Board) Director oversees the ethical review process for research involving human subjects, ensuring compliance with federal regulations and institutional policies. They manage the IRB office, coordinate board meetings, review protocols, and provide guidance to researchers on ethical issues. The IRB Director also ensures that research projects adhere to ethical standards, maintains documentation, and facilitates training for staff and researchers. Their role is critical in protecting the rights and welfare of human subjects in research.

What are the main responsibilities of an IRB director in a typical week?

As an IRB Director, you can expect to oversee research protocol reviews, ensure adherence to regulatory and ethical standards, and facilitate meetings with board members. Your week may involve providing guidance to investigators, training staff on compliance issues, and coordinating with legal, medical, and research professionals to address complex ethical questions. Many IRB Directors also play a role in policy development and ongoing process improvements. This role requires balancing administrative duties with hands-on oversight to ensure that all human subjects research meets the highest standards of safety and ethics.

What are the key skills and qualifications needed to thrive in the IRB director position, and why are they important?

To thrive as an IRB Director, you need in-depth knowledge of human subjects research regulations, attention to detail, and experience in research ethics, typically supported by an advanced degree in a relevant field. Proficiency with electronic IRB management systems, compliance tracking software, and certification such as CIP (Certified IRB Professional) are commonly required. Outstanding leadership, communication, and problem-solving abilities help IRB Directors effectively manage review panels and address complex ethical considerations. These skills ensure the integrity and compliance of research involving human subjects while fostering a culture of ethical oversight.

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Irb Director jobs near you
Infographic showing various Irb Director job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $90,903 per year, or $43.7 per hour.

Clinical Research Site Director

ObjectiveHealth

Little Rock, AR • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Job description

Clinical Research Site Director
ObjectiveHealth is currently seeking a qualified candidate for the full-time position of Clinical Research Site Director. The ideal candidate will have prior experience in site leadership and 5 years of experience coordinating industry-sponsored clinical trials.
Who We Are
ObjectiveHealth is a clinical research company that uses proprietary technology to:
  1. Increase patient access to research trials within our communities,
  2. Provide physicians with enhanced care options for current patients, and
  3. Deliver superior clinical research enrollment metrics to Pharma sponsors.

All with the goal of Improving Patient Outcomes at the point of care.
We want you to join us in doing just that.
Who You Are
  • A lover of patient interaction and skilled at providing patient care
  • A team player with a bias for action and an attitude that takes personal responsibility
  • A proven leader among your peers and teams
  • Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
  • Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
  • Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
  • An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
  • A strong advocate for Company values, mission, and initiatives
  • Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
  • Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or Oncology

What Success Looks Like for This Role
  • Taking ownership of assigned studies and patients
  • Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
  • Showing up on time, every time
  • Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
  • Learning and using the technologies we provide to enhance your day-to-day activities
  • Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

What We Offer
Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.
Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas.
ObjectiveHealth is an EEO Employer and an E-Verify participant.

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