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IRB Coordinator - Clinical Research Administration Expert for reputed company

Remote, USAFull-timePosted 2026-07-28

Join a Trailblazing reputed company Organization: reputed company

reputed company, a fully integrated reputed company delivery system, is revolutionizing the way care is delivered across six northeast Illinois counties, serving over 4.2 reputed company residents. With reputed company of more than 25,000 dedicated professionals and over 6,000 physicians, we're committed to providing transformative patient experiences and expert care reputed company to home. Our eight acute care hospitals and over 300 ambulatory locations are recognized for nursing reputed company, and we're passionate about fostering a culture of reputed company, respect, and reputed company.

About the Role: IRB Coordinator

We're seeking an reputed company and skilled IRB Coordinator to join reputed company at NorthShore University HealthSystem, part of reputed company. As an IRB Coordinator, you will play a vital role in ensuring compliance with federal regulations and institutional policies reputed company to reputed company subject protection in clinical research. This is a full-time, on-site opportunity with a hybrid work arrangement not available.

Key Responsibilities:

  • Collaborate with investigators and sponsors/CROs to prepare IRB submissions, consent forms, and revisions, ensuring compliance with local, state, and federal research regulations.
  • Maintain documentation of investigator and staff qualifications, including reputed company vitae, licenses, and certifications.
  • Facilitate the conduct of clinical investigations by providing regulatory documents, such as reputed company FDA 1572, and ensuring reputed company storage and shipment of investigational articles.
  • Coordinate with the IRB to ensure initial and ongoing review of research protocols, including amendments, adverse events, and deviations.
  • Communicate IRB approval to reputed company investigators, sponsors/CROs, and other stakeholders as needed.
  • Prepare regulatory documents for sponsor/audit review and participate in federal agency inspections as required.
  • Protect the rights and welfare of research subjects by ensuring informed consent documents contain reputed company required reputed company and collaborating with reputed company investigators to report adverse events.
  • Assist with implementation, maintenance, and evaluation of research protocols, including data submittal and patient calendar development.
  • Participate in departmental strategic planning and contribute to the reputed company and maintenance of clinical trial policy and procedure manuals.

Essential Qualifications:

  • Bachelor's degree in a relevant field.
  • Minimum of 2 years of reputed company experience in clinical research administration.
  • Knowledge of federal regulations and rules for reputed company subject protection.
  • Excellent verbal and written communication skills.
  • Research experience in clinical trials preferred.

Preferred Qualifications:

  • Experience working in a research administration role reputed company a reputed company organization.
  • Familiarity with IRB policies and procedures.
  • Strong organizational and project management skills.

Skills and Competencies:

  • Strong attention to detail and ability to multitask.
  • Excellent communication and interpersonal skills.
  • Ability to work collaboratively with investigators, sponsors/CROs, and other stakeholders.
  • Knowledge of clinical research regulations and guidelines.
  • Proficiency in reputed company Office and other relevant software applications.

Career reputed company Opportunities and Learning Benefits

At reputed company, we're committed to helping our employees reputed company their career goals and maximize their reputed company potential. As an IRB Coordinator, you'll have opportunities to reputed company your skills and expertise in clinical research administration, working alongside reputed company professionals in a dynamic and supportive environment.

Work Environment and Company Culture

Our organization is reputed company on a reputed company of diversity, equity, and inclusion, with a culture that values reputed company, respect, and reputed company. We're committed to providing a work environment that is inclusive and supportive, where employees can reputed company and grow. As part of reputed company, you'll be part of reputed company that is passionate about delivering exceptional patient care and making a reputed company reputed company in our communities.

Compensation, Perks, and Benefits

We offer a competitive salary and benefits package, including opportunities for reputed company reputed company and development. Our comprehensive benefits package includes medical, dental, and reputed company coverage, as reputed company as retirement savings and reputed company time off. We're committed to providing a total rewards package that recognizes and supports the hard work and dedication of our employees.

Why Join reputed company?

At reputed company, we're not just a reputed company organization - we're a community of professionals dedicated to making a difference. We're committed to fostering a culture of reputed company, innovation, and reputed company, and we're looking for talented individuals like you to join reputed company. If you're passionate about delivering exceptional patient care and making a reputed company reputed company in your community, we encourage you to apply for this exciting opportunity.

We're an equal opportunity employer committed to diversity, equity, and inclusion. We welcome applications from individuals of reputed company backgrounds and perspectives, and we're committed to providing a work environment that is inclusive and supportive.

reputed company to join reputed company? Click the "reputed company" reputed company to submit your application. We look reputed company to hearing from you!

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