Senior Human Research Protection Program (Hrpp) Administrator-4

Brown University; Providence (RI); Remote; USD 110,000 - 125,000; Full time

Benefits offered by this job

Health benefits

Retirement options

Tuition assistance

Wellness programs

Job summary

Brown University is seeking a Senior HRPP Administrator to lead the administration and implementation of the Human Research Protection Program (HRPP) and IRB policies across Brown University, Lifespan, and Care New England.

This role ensures compliance with federal and state regulations, supports IRB committee meetings, prepares meeting agendas and minutes, and advises on applicable review criteria. A strong understanding of regulatory requirements and institutional policies is essential.

Qualifications

• Bachelor's degree and 5+ years of related experience or equivalent combination.
• In-depth understanding of applicable laws, regulations, and policies related to human subjects research, including FDA regulations.
• Experience in academic or clinical research settings.
• CIP certification or willingness/ability to obtain CIP within two years preferred.

Responsibilities

• Lead administration and implementation of HRPP and IRB policies for Brown University, Lifespan, and Care New England.
• Support IRB Committee meetings, prepare agendas and minutes, and advise on review criteria.
• Maintain up-to-date knowledge of federal, state, and institutional policies governing human subjects research.
• Collaborate with faculty, staff, and students to ensure compliant research conduct.

Skills

Attention to detail

Regulatory compliance

Communication

Project management

Collaboration

Education

Bachelor's degree

5+ years related experience

Tools

IRB submission system

Job description

Senior Human Research Protection Program (Hrpp) Administrator-4

Job Description

About Brown

Brown University is a leading research university distinct for its student-centered learning and deep sense of purpose. Our students, faculty and staff are driven by the idea that their work will have an impact in the world. Brown University offers a flexible work/life balance; summer hours, winter break and a comprehensive Benefits package including time off, annual paid holidays; benefits offerings including health, dental, vision, tuition assistance, retirement, wellness, employee discounts and more. To learn about Brown University's benefits, visit the University Human Resources web page for further information.

About the Opportunity

The Senior HRPP Administrator is responsible for the administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board (IRB) policies and procedures related to the conduct of human subjects research studies at Brown University, Lifespan, and Care New England. The Senior HRPP Administrator ensures that all biomedical and behavioral human subjects research activities conducted at Brown University, Lifespan, and/or Care New England comply with federal regulations, state and local law, institutional policies, and AAHRPP accreditation standards. The Senior HRPP Administrator conducts non-committee reviews and works collaboratively and independently with faculty, staff, and students. This role supports IRB Committee meetings, is responsible for preparing meeting agendas and materials, taking minutes, and advising IRB members on applicable regulations, policies, and review criteria. This position maintains a knowledge and understanding of current federal, state regulations, state and local law, and institutional policies and departmental SOPs.

Education and Experience

Required:

• Bachelor's degree and 5+ years of related experience or equivalent combination of education and experience.
• In-depth understanding of applicable laws, regulations, and policies related to human subjects research, including FDA regulations.
• Experience working in an academic or clinical research setting.

Preferred:

• CIP certification or willingness/ability to obtain CIP certification within two years of hire.
• Knowledge of clinical trials, clinical trial registration, and clinical trial results reporting is highly desirable.
• Must demonstrate an in-depth understanding of operational requirements pertaining to the management and implementation of protocol review processes.
• Comfortable managing and performing work in an electronic system.

Job Competencies

• In-depth understanding of current federal and State regulations regarding human subjects research and ethical principles, Institutional policies, and integrated HRPP SOPs;
• Ability to practically apply federal and state regulations as well as institutional policies to research submissions under review
• Ability to independently and competently handle protocol reviews
• Ability to handle confidential documents and sensitive information
• Experience with high volumes and rigid deadlines while maintaining attention to detail
• Ability to multitask and prioritize workloads
• Excellent interpersonal, oral and written communication skills
• Ability to work independently and use judgment and discretion in potentially controversial matters
• Ability to work with little supervision and also serve as a strong team member
• Participation in continuing education and national and/or regional organizations devoted to promoting research ethics and the protection of human subjects
• Proficiency in an electronic IRB submission system, Microsoft Office applications, Google platforms, Adobe and other commonly used software;

Additional Information

• Applicants are asked to include a resume and cover letter with their application.
• All offers of employment are contingent upon a criminal background check and education verification satisfactory to Brown University.
• The successful candidate must reside in a state in which Brown is registered to conduct business.

Benefits of Working at Brown:

Please review additional information on the Benefits of Working at Brown.

Employment Details

Worker Type: Employee

Worker Sub-Type: Regular

Time Type: Full time

Scheduled Weekly Hours: 37.5

Position Work Location: Remote

Submission Guidelines

The designated Position Work Location for each position determines the approved modality of work. Positions are classified based on the operational and business needs of the department and may be designated as on-site, hybrid, or remote. Employees with a designated position work location as remote must reside and perform their work in a state where Brown University is registered to do business. Brown University is a registered employer in the following states: Rhode Island, California, Colorado, Connecticut, Florida, Maryland, Massachusetts, New York, New Hampshire, New Jersey, North Carolina, Washington, D.C.

Eligibility

This position is not eligible for visa sponsorship.

Still Have Questions?

If you have any questions you may contact [e-mail].

Brown is an E-Verify Employer.

EEO Statement:

Brown University provides equal opportunity and prohibits discrimination, harassment and retaliation based upon a person's race, color, religion, sex, age, national or ethnic origin, disability, veteran status, sexual orientation, gender identity, gender expression, or any other characteristic protected under applicable law, in the administration of its policies, programs, and activities. The University recognizes and rewards individuals on the basis of qualifications and performance. The University maintains certain affirmative action programs in compliance with applicable law.