Human Research Protection Program Coordinator

Texas A&M University; College Station (TX); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health benefits

Paid holidays

PTO and leave benefits

Retirement plan

LinkedIn Learning

Job summary

Texas A&M University in College Station seeks a motivated Human Research Protection Program Coordinator to support ethical, compliant studies involving human participants. You will coordinate IRB reviews, advise investigators, and ensure regulatory alignment.

The role requires a master's in a health-related or regulatory field, experience in human subjects research compliance, and CIP or CCRP certification. Strong communication and teamwork are essential in a fast-paced environment.

Qualifications

• Bachelor's degree in science, biomedical, health-related, or regulatory field.
• Three years of experience in compliance/regulations, auditing, legal work, research, medical, scientific writing, clinical trials or related.
• Preferred: Master’s degree in health related or regulatory field.
• A minimum of one year of experience in human subject research compliance and two years in a related area social & behavioral or biomedical research or clinical trials management.
• Certified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP)

Responsibilities

• Coordination and Protocol Review: Coordinates all aspects of the IRB review based on knowledge of institutional guidelines and federal regulations.
• Consults and advises faculty, staff, and students in the preparation of protocol applications.
• Provides pre-reviews of protocols including determinations of exempt status.
• HRPP Resources & Contact: Provides expertise about human subjects' research to investigators and committee members related to regulatory and institutional guidelines.
• Responsible for effective communication and timely responses related to research reviews.
• Responds to questions regarding the HRPP compliance program.
• IRB Support: Provides coordination and support for the IRB.
• Prepares for meetings by organizing review materials, agendas, and other meeting related documents.
• Performs post-review functions by preparing correspondence, minutes, and other reports based upon IRB determinations.
• Assists supervisor in the development or modification of standard business practices and office processes related to HRPP functions.
• Records Management: Provides quality assurance oversight of data entry related to research submissions, reports, and notices.
• Maintains electronic and paper files ensuring all are accurate and complete.
• Training and Development: Assists the supervisor in the development of training materials or administrative processes.
• Conducts and participates in regulatory training or outreach activities as needed.

Skills

Analytical skills

Interpersonal skills

Regulatory knowledge

Communication skills

Education

Bachelor's degree in science/biomedical/health-related/regulatory field

Master's degree in health-related or regulatory field

Certified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP)

Tools

Word

Excel

Access

Adobe

Job description

Job TitleHuman Research Protection Program Coordinator Agency Texas A&M University Department Research Compliance & Biosafety Program Proposed Minimum SalaryCommensurate Job LocationCollege Station, Texas Job TypeStaff

Job Description

Who We Are

The Human Research Protection Program (HRPP) supports Texas A&M University's commitment to excellence in research by helping ensure studies involving human participants are conducted ethically, responsibly, and in compliance with regulatory requirements. Through collaboration, education, and service, we empower researchers to make meaningful discoveries while safeguarding the individuals who make that research possible.

What We Want

We are seeking a collaborative and detail-oriented professional who is passionate about supporting ethical, high-quality research. The ideal candidate brings a master's degree in a health-related or regulatory field, experience in human subjects research compliance and related areas such as social and behavioral research, biomedical research, or clinical trials management, and a professional certification such as a Certified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP). Successful candidates enjoy interpreting complex requirements, providing exceptional customer service, building strong partnerships with faculty, staff, and students, and serving as a trusted resource on research compliance matters. If you thrive in a fast-paced environment, can balance multiple priorities, and are motivated by helping researchers advance meaningful discoveries while protecting the rights and welfare of research participants, we'd love to hear from you.

What You Need To Know

Salary: Commensurate

Qualifications Required

• Bachelor’s degree in science, biomedical, health-related, or regulatory field.
• Three years of experience in compliance/regulations, auditing, legal work, research, medical, scientific writing, clinical trials or related.
• Preferred Qualifications Master’s degree in health related or regulatory field.
• A minimum of one year of experience in human subject research compliance and two years in a related area social & behavioral or biomedical research or clinical trials management.
• Certified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP)

Knowledge, Skills, and Abilities

• Knowledge of the federal regulations regarding human subjects, including HHS and FDA.
• Ability to demonstrate analytical skills, gather, interpret, organize, and present complex research compliance data.
• Demonstrated success working collaboratively with interdisciplinary teams of external and internal individuals.
• Must be well organized.
• Strong interpersonal and communication skills.
• Knowledge of standard software, such as Word, Excel, Adobe, and Access.
• Ability to multi-task and work cooperatively with others.

Responsibilities

• Coordination and Protocol Review Coordinates all aspects of the IRB review based on knowledge of institutional guidelines and federal regulations.
• Consults and advises faculty, staff, and students in the preparation of protocol applications.
• Provides pre-reviews of protocols including determinations of exempt status.
• HRPP Resources & Contact Provides expertise about human subjects' research to investigators and committee members related to regulatory and institutional guidelines.
• Responsible for effective communication and timely responses related to research reviews.
• Responds to questions regarding the HRPP compliance program.
• IRB Support Provides coordination and support for the IRB.
• Prepares for meetings by organizing review materials, agendas, and other meeting related documents.
• Performs post-review functions by preparing correspondence, minutes, and other reports based upon IRB determinations.
• Assists supervisor in the development or modification of standard business practices and office processes related to HRPP functions.
• Records Management Provides quality assurance oversight of data entry related to research submissions, reports, and notices.
• Maintains electronic and paper files ensuring all are accurate and complete.
• Training and Development Assists the supervisor in the development of training materials or administrative processes.
• Conducts and participates in regulatory training or outreach activities as needed.

Why Texas A&M University?

We are a prestigious university with strong traditions, Core Values, and a community of caring and collaboration.Amenities associated with a major university, such as sporting and cultural events, state-of-the-art recreation facilities, the Bush Library and Museum, and much more await you. Experience all that a big city has to offer but with a reasonable cost-of-living and no long commutes.

• Medical, prescription drug, dental, vision, life and AD&D, flexible spending accounts, and long-term disability insurance with Texas A&M contributing to employee health and basic life premiums
• 12-15 days of annual paid holidays
• Up to eight hours of paid sick leaveand at leasteight hours of paid vacationeach month
• Automatic enrollment in theTeacher Retirement System of Texas
• Health and Wellness: Free exercise programs and release time
• Professional Development: All employees have access to freeLinkedIn Learningtraining, webinars, and limited financial support to attend conferences, workshops, and more
• Educational release time and tuition assistancefor completing a degree while a Texas A&M employee
• Living Well, a program at Texas A&M that has been built by employees, for employees

Our Commitment

Texas A&M University is committed to enriching the learning and working environment by promoting a culture that respects all perspectives, talents & lived experiences. Embracing varying opinions and perspectives strengthens our core values which are: Respect, Excellence, Leadership, Loyalty, Integrity, and Selfless Service.

Equal Opportunity/Veterans/Disability Employer.

All positions are security-sensitive. Applicants are subject to a criminal history investigation, and employment is contingent upon the institution’s verification of credentials and/or other information required by the institution’s procedures, including the completion of the criminal history check.

Howdy and thank you for your interest in a career with Texas A&M University. As the flagship campus of The Texas A&M University System, we are located in College Station, Texas with a student population of more than 74,000 and nearly 14,000 faculty and staff. The Spirit of Aggieland is unmistakable. We are a unique American institution, fostering a culture of friendliness, compassion and respect for one another. Our unique history and rich traditions make Texas A&M special. From our benefits package and professional development opportunities to our retirement programs, Texas A&M is a great place to work. Your path to a great career starts here! Equal Opportunity/Veterans/Disability Employer.