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.

Who We Are

The Human Research Protection Program (HRPP) is composed of institutional leaders, research review committees, and agents of Texas A&M University that are responsible for protecting the rights and welfare of participants in research conducted or reviewed by Texas A&M University, including Texas A&M Health and all of its locations, the School of Law, and branch campuses in Galveston.

What We Want

The Senior Research Compliance Coordinator, under general supervision, provides advanced protocol review and advises and assists investigators, administrators, and others on the requirements of human subjects research, biomedical or behavioral clinical trials, FDA IND/IDE regulations and single IRB processes. Assists and educates investigators on Good Clinical Practice requirements and investigator responsibilities including regulatory file set-up.

What You Need To Know

Commensurate with experience, salary range: $86,403.12 - $95,043.36

A cover letter and resume are required.

Position Details: Hybrid Work Option: Due to the nature of this position, a hybrid work arrangement may be available for workplace flexibility.

Required Education and Experience

• Bachelor's degree in applicable field or equivalent combination of education and experience.

• Four years of experience in industry or federally supported clinical trials, investigator-initiated clinical research, or within a compliance or administrative group focused on regulatory support, clinical operations, or clinical research.

Required Knowledge, Skills, and Abilities

• Ability to effectively communicate with a broad spectrum of constituents, including faculty members, students, high-level administrators, and IRB staff.

• Knowledge of word processing, spreadsheet, and database applications.

• Ability to multitask and work cooperatively with others. Effective interpersonal and organizational skills.

Preferred Qualifications

• Master’s degree in education, business, research, or science related field.

• Any of the following: Certified IRB Professional (CIP), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) Certified Clinical Trials Manager (CTM)

• Knowledge of biomedical and behavioral research including clinical trials.

• Knowledge of regulations and ethical principles regarding research including HIPAA, FDA, OHRP and FERPA in addition to above knowledge, skills and abilities.

• Ability to cultivate and maintain professional working relationships with people of varying backgrounds.