Serve as liaison between IRB and investigators. • Assist in the development or revision of HRPP ... Ability to collect, analyze and incorporate additional technical information from a variety of ...
Serve as liaison between IRB and investigators. • Assist in the development or revision of HRPP ... Ability to collect, analyze and incorporate additional technical information from a variety of ...
MRI Research Assistant - Radiology
La Jolla, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
MRI Research Assistant - Radiology
La Jolla, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
MRI Research Assistant - Radiology
San Diego, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
MRI Research Assistant - Radiology
San Diego, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Serves as site inspection or assist visit team member for other HRPP staff members, as needed. * Performs full range of subject matter research and analyses. * Interprets results to determine ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Serves as site inspection or assist visit team member for other HRPP staff members, as needed. * Performs full range of subject matter research and analyses. * Interprets results to determine ...
MRI Research Assistant - Radiology
San Diego, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
MRI Research Assistant - Radiology
San Diego, CA · On-site
$30.12 - $35.93/hr
Create and maintain regulatory documents in accordance with UCSD HRPP guidelines and the department ... Knowledge to work with and learn new software for analysis. * Demonstrated skill in accurate record ...
Clinical Research Quality Assurance and Improvement Specialist
Chicago, IL · On-site
$37.75 - $50.25/hr
... HRPP). Assists with preparation for external quality reviews and regulatory audits.**Essential Job Functions:**1. Utilizes expert knowledge to analyze and interpret applicable regulations (federal ...
Clinical Research Quality Assurance and Improvement Specialist
Chicago, IL · On-site
$37.75 - $50.25/hr
... HRPP). Assists with preparation for external quality reviews and regulatory audits.**Essential Job Functions:**1. Utilizes expert knowledge to analyze and interpret applicable regulations (federal ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Serves as site inspection or assist visit team member for other HRPP staff members, as needed. * Performs full range of subject matter research and analyses. * Interprets results to determine ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Serves as site inspection or assist visit team member for other HRPP staff members, as needed. * Performs full range of subject matter research and analyses. * Interprets results to determine ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Administer and continuously improve HRPP operations, including oversight of intake processes, workflow design, compliance tracking, reporting, metrics analysis, and development of operational tools ...
Clinical Research Monitor
Manhattan, NY · On-site
... HRPP * Assists with compliance training initiatives including coordinating educational sessions ... Strong analytical and problem solving skills, excellent interpersonal and communications skills ...
Clinical Research Monitor
Manhattan, NY · On-site
... HRPP * Assists with compliance training initiatives including coordinating educational sessions ... Strong analytical and problem solving skills, excellent interpersonal and communications skills ...
Associate Director, Office for Human Research Studies
Brookline, MA · On-site +1
$106K - $118K/yr
The Associate Director is a member of the OHRS Senior Staff and reports to the Director, HRPP. The Associate Director supervises Senior IRB Analysts and protocol-focused IRB Analysts. The Associate ...
Associate Director, Office for Human Research Studies
Brookline, MA · On-site +1
$106K - $118K/yr
The Associate Director is a member of the OHRS Senior Staff and reports to the Director, HRPP. The Associate Director supervises Senior IRB Analysts and protocol-focused IRB Analysts. The Associate ...
Clinical Research Coordinator I
Dallas, TX · On-site
$24 - $32/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Clinical Research Coordinator I
Dallas, TX · On-site
$24 - $32/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Clinical Research Monitor
Manhattan, NY · On-site
$43.68 - $50.77/hr
... HRPP * Assists with compliance training initiatives including coordinating educational sessions ... Strong analytical and problem solving skills, excellent interpersonal and communications skills ...
Clinical Research Monitor
Manhattan, NY · On-site
$43.68 - $50.77/hr
... HRPP * Assists with compliance training initiatives including coordinating educational sessions ... Strong analytical and problem solving skills, excellent interpersonal and communications skills ...
The Associate Director is a member of the OHRS Senior Staff and reports to the Director, HRPP. The Associate Director supervises Senior IRB Analysts and protocol-focused IRB Analysts. The Associate ...
The Associate Director is a member of the OHRS Senior Staff and reports to the Director, HRPP. The Associate Director supervises Senior IRB Analysts and protocol-focused IRB Analysts. The Associate ...
Clinical Research Coordinator - Pediatrics
Hershey, PA · On-site
$23 - $30.50/hr
... analysis, and regulatory/ethics procedures, and a demonstrated interest in pediatric oncology ... HRPP); and foster effective relationships with regulatory agencies, research organizations, and ...
Clinical Research Coordinator - Pediatrics
Hershey, PA · On-site
$23 - $30.50/hr
... analysis, and regulatory/ethics procedures, and a demonstrated interest in pediatric oncology ... HRPP); and foster effective relationships with regulatory agencies, research organizations, and ...
Work with appropriate internal resources to analyze data and prepare and present Institutional ... HRPP). * Design, implement and evaluate organizational and staffing models to effectively ...
Work with appropriate internal resources to analyze data and prepare and present Institutional ... HRPP). * Design, implement and evaluate organizational and staffing models to effectively ...
Clinical Research Coordinator II, Pediatrics
Dallas, TX · On-site
$24 - $32/hr
Familiarity with data analysis or visualization tools such as R, Stata, SAS, GraphPad Prism, or ... and HRPP standards. * May perform research billing activities, as needed, based on size of ...
Clinical Research Coordinator II, Pediatrics
Dallas, TX · On-site
$24 - $32/hr
Familiarity with data analysis or visualization tools such as R, Stata, SAS, GraphPad Prism, or ... and HRPP standards. * May perform research billing activities, as needed, based on size of ...
Clinical Research Coordinator I
Dallas, TX · On-site
$60 - $80/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Clinical Research Coordinator I
Dallas, TX · On-site
$60 - $80/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Clinical Research Coordinator I
Dallas, TX · On-site
$24 - $32/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Clinical Research Coordinator I
Dallas, TX · On-site
$24 - $32/hr
This role will also perform QA/QC clinical analysis and data checks using various databases based ... HRPP standards. * Review research study protocols to ensure feasibility * Assist in developing ...
Hrpp Analyst information
See salary details
$33K - $41.3K
2% of jobs
$41.3K - $49.5K
10% of jobs
$56.9K is the 25th percentile. Wages below this are outliers.
$49.5K - $57.8K
15% of jobs
$57.8K - $66.1K
18% of jobs
The median wage is $68.7K / yr.
$66.1K - $74.4K
17% of jobs
$74.4K - $82.6K
11% of jobs
$84.9K is the 75th percentile. Wages above this are outliers.
$82.6K - $90.9K
10% of jobs
$90.9K - $99.2K
9% of jobs
$99.2K - $107.5K
2% of jobs
$107.5K - $115.7K
2% of jobs
$115.7K - $124K
5% of jobs
$33K
$76.3K
$124K
How much do hrpp analyst jobs pay per year?
What is an HRPP analyst?
What are the key skills and qualifications needed to thrive as an HRPP analyst?
What are the primary challenges HRPP analysts face when ensuring compliance with human research protection regulations?
What is the difference between Hrpp Analyst vs Compensation Analyst?
| Aspect | Hrpp Analyst | Compensation Analyst |
|---|---|---|
| Credentials | Bachelor's degree, HR or related certifications | Bachelor's degree, HR or finance certifications often preferred |
| Work Environment | HR departments, corporate offices | HR or compensation departments, corporate offices |
| Industry Usage | Used across various industries for HR processes | Primarily in HR and compensation-focused roles |
| Search & Comparison Intent | Understanding HR-related roles and responsibilities | Focusing on salary structures and benefits analysis |
While both roles involve HR functions, an Hrpp Analyst focuses on payroll processing, compliance, and HR data management, whereas a Compensation Analyst specializes in salary structures, benefits, and compensation strategies. The roles often overlap but serve distinct functions within HR departments.
What are popular job titles related to Hrpp Analyst jobs?
For Hrpp Analyst jobs, the most frequently searched job titles are:

Administrator II (IRB) (210-2026-41)
Orangeburg, NY
Full-time
Retirement
Re-posted 13 days ago
Key responsibilities
Assist with the processing of protocol submissions and maintain IRB files.
Facilitate IRB meetings, prepare agendas, and document meeting minutes according to federal guidelines.
Provide guidance to research teams on IRB regulations, ethical conduct, and compliance requirements.
Job description
JOB DESCRIPTION:
This position at the Nathan Kline Institute (NKI) involves working within a research enterprise by serving as an integral component of a human research protection program.
The incumbent is required to maintain an understanding of IRB regulations to help ensure the continued success of the NKI IRB. The incumbent is responsible for educating research teams on the proper conduct and ethical treatment of research participants and research data. Responsibilities include assisting with timely processing of protocol submissions, maintaining IRB files, tracking metrics of IRB performance, and coordinating IRB meetings. Job duties also include documentation of IRB minutes per federal guidelines and knowledge and awareness of all guidelines associated with minimal risk research and IRB minutes documentation. The incumbent must also be prepared to interface with research projects conducted under guidelines for clinical research and FDA requirements under the supervision of the IRB director or designee.
This position permits up to 50 % of schedule to be worked remotely.
JOB DUTIES:
• Conduct pre-review of human subjects research submissions, not human subjects research, reliance, and QI/QA projects and prepare materials for primary reviewers.
• Facilitate full IRB review per HRPP policies, state law, and federal regulations.
• Attend and participate in IRB Committee meetings.
• Ensure research requests are compliant with all applicable institutional policy, state laws and federal regulations.
• Determine IRB requirements of approval are met for human subjects research requests.
• Maintain clear and accurate IRB files both electronic and hard copies.
• Provide support and guidance to investigators from initial proposal review and submission through completion of the study. Serve as liaison between IRB and investigators.
• Assist in the development or revision of HRPP policies, procedures, forms, and checklists as necessary.
• Participate in on-line training, webinars, and in-person education as required by the HRPP.
• Prepare and modify documents including correspondence, reports, drafts, memos, and emails.
• Prepare agendas for meetings and distribute minutes of meetings.
• Maintenance of the NKI education requirements for all research.
• Prepare IRB Meeting Minutes
• Other duties as assigned by the supervisor
JOB QUALIFICATIONS:
Minimum Qualifications:
• BA or BS or equivalent background and experience, preferably in life, physical or social science.
• At least 1 year IRB staff experience
• Working knowledge of ethical principles and regulatory information regarding the protection of human research participants (DHHS and FDA).
• Understanding of the operational requirements related to the management and implementation of the IRB review process.
• Demonstrated excellent oral and written communication, problem solving and analytical skills necessary to quickly identify and synthesize salient features from a fast-paced discussion of highly technical broad-ranging information into a cohesive and well-written correspondence to researchers and other audiences. Ability to collect, analyze and incorporate additional technical information from a variety of sources into this process.
• Excellent interpersonal skills, political acumen and tact needed to work with a wide variety of customers, including faculty members, research staff, students, IRB members and Chair persons, with colleagues and managers, and with external parties such as government officials in a consistently professional and service-oriented manner.
• Ability to work with an electronic IRB review system; guide or provide assistance to others using the system for IRB submission, review and approval.
• Ability to maintain strict standards of confidentiality in dealing with protected information.
Background Investigation/Justice Center Review Requirements:
Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Prospective employees whose names appear on the SEL as having been found responsible for serious or repeated acts of abuse or neglect will be barred from appointment. 2) Screened against the Statewide Central Register of Child Abuse and Maltreatment (SCR). Prospective employees whose names are indicated on the SCR may be barred from appointment.
*The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.
Applications will only be accepted through website at: http://corporate.rfmh.org - Click on Employment Opportunities. Applications will be accepted only during the posting dates as listed at the top of the job announcement.
Questions regarding this position please email: hrprocessing@nki.rfmh.org
About Research Foundation for Mental Hygiene
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