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Human Research Protection Program Coordinator

Texas A&M University System

College Station, TXFull-timeSeen 6 days agoSeen in employer's feed 6 days ago

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At a glance

Compensation
No compensation found
Location
College Station, TX
Schedule
Full-time
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Human Research Protection Program Coordinator at Texas A&M University supports ethical human subjects research by coordinating IRB reviews, advising investigators, and ensuring compliance with federal regulations while providing excellent customer service and collaborative partnership across the university community.

Skills & qualifications

RequiredNice to have

Skills

WordExcelAdobeAccessFederal Regulations KnowledgeAnalytical SkillsInterpersonal SkillsCommunication Skills

Qualifications

Bachelor's Degree in Science, Biomedical, Health-Related, or Regulatory FieldThree Years Experience in Compliance/Regulations, Auditing, Legal Work, Research, Medical, Scientific Writing, Clinical Trials or RelatedMaster's Degree in Health Related or Regulatory FieldOne Year Experience in Human Subject Research ComplianceTwo Years Experience in Social & Behavioral or Biomedical Research or Clinical Trials ManagementCertified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP)Well Organized

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off
Tuition Assistance

Full job description

College Station, TX

Full time

R-096716

Job Title

Human Research Protection Program Coordinator

Agency

Texas A&M University

Department

Research Compliance & Biosafety Program

Proposed Minimum Salary

Commensurate

Job Location

College Station, Texas

Job Type

Staff

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

Special Note: A cover letter and resume are strongly recommended.

Qualifications

Required Education and Experience

  • 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 such 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.

Our Commitment

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

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.

Equal Opportunity/Veterans/Disability Employer.

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.

If you need assistance in applying for this job, please contact (979) 845-5154.

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