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Human Research Protection Program Irb Manager Jobs

... in human research. This job will also include career development mentoring and opportunities for ... This individual will schedule and participate in all sponsor and/or IRB monitoring visits to review ...

... in human research. This job will also include career development mentoring and opportunities for ... This individual will schedule and participate in all sponsor and/or IRB monitoring visits to review ...

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Human Research Protection Program Irb Manager information

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$50K

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How much do human research protection program irb manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for human research protection program irb manager in the United States is $98,569.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $114,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Human Research Protection Program Irb Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $98,569 per year, or $47.4 per hour.

Research Coordinator/Therapist

Salt Lake City, UT โ€ข On-site

The Chronicle Of Higher Education, Inc.
Newspaper Publishersย โ€ขย 201 - 500 employees

$100/hr

Other

Posted 10 days ago


Key responsibilities

  • Conduct patient evaluations and provide study-related treatment interventions in accordance with approved study protocols.

  • Document assessments, treatments, participant responses, and relevant findings to support study implementation and data integrity.

  • Report adverse events, document protocol deviations, and prepare summary reports for the sponsor.


Job description

Overview

Research Coordinator/Therapist role. Provides assessment and treatment to patients in a clinical research study. Assists the Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.

Entry-level Masterโ€™s or Doctorate in Occupational Therapy or Physical Therapy. IRB CITI Course in the Protection of Human Research Subjects certificate obtained within six months of hire, and demonstrated human relations and effective communication skills are required.

This position is patient-sensitive and requires vaccination according to CDC standards and hospital policy, with exemptions possible for documented medical contraindications or religious beliefs that object to vaccinations. All patient-sensitive employees must be immunized unless exempted.

Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.

This description indicates the general nature and level of work performed by employees within this classification and is not a comprehensive inventory of all duties, responsibilities, and qualifications.

Incumbents are responsible for coordinating the daily operations of their assigned research team, ensuring safe and orderly flow of the research project and maintaining adequate resources for the PI to accomplish research objectives.

Hourly salary: $50/hour with a maximum of $100/hour for a 2 hour treatment session.

Responsibilities
  • Conduct patient evaluations and provide study-related treatment interventions in accordance with approved study protocols, ensuring consistency, participant safety, and protocol adherence.
  • Document all assessments, treatments, and participant responses accurately, and communicate relevant findings to the research team to support study implementation and data integrity.
  • Ensure accurate documentation, maintain confidentiality of protected health information, and collaborate with investigators and study staff to facilitate efficient participant recruitment. Mileage will be reimbursed for work-related travel (e.g., participant recruitment and outreach activities).
  • Attend and participate in Investigator and staff meetings. Advise the team regarding specific study assignments and timelines.
  • Determine length of visits and coordinate participantsโ€™ schedules with the study team.
  • Report and track adverse events (AE). Report serious AEs to IRB and sponsor.
  • Document all protocol deviations, reconcile test article accountability at study close out, and prepare summary reports for sponsor.
  • Complete, audit, correct Case Report Forms (CRFs), and relay CRFs to sponsor.
  • May perform functions required of the Clinical Research Assistant as necessary.
Minimum Qualifications

Equivalency Statement: 1 year of higher education can be substituted for 1 year of directly related work experience (example: bachelorโ€™s degree = 4 years of directly related work experience).

Job Levels:

  • Research Coordinator (Non-R.N.), V: Requires a bachelorโ€™s (or equivalency) + 10 years or a masterโ€™s (or equivalency) + 8 years of directly related work experience.
  • Research Coordinator (Non-R.N.), VI: Requires a bachelorโ€™s (or equivalency) + 12 years or a masterโ€™s (or equivalency) + 10 years of directly related work experience.
  • Research Coordinator (Non-R.N.), VII: Requires a bachelorโ€™s (or equivalency) + 14 years or a masterโ€™s (or equivalency) + 12 years of directly related work experience.
Preferences Details
  • Special Instructions: Apply with resume, cover letter, and three references.
  • Requisition Number: PRN17231N
  • Full Time or Part Time? Part Time
  • Work Schedule Summary: Flexible
  • Department: 00204 - Occupational/Recreational Therapy
  • Location: Campus
  • Pay Rate Range: up to $50/hr
  • Close Date: 10/14/2026
  • Open Until Filled: Yes
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