23 часа назад
Human Research Protection Program Coordinator
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Human Research Protection Program Coordinator (Research Compliance): Coordinating IRB reviews and supporting ethical, compliant research involving human participants with an accent on federal regulations, protocol assessment, and investigator guidance. Focus on interpreting complex compliance requirements, organizing review materials, maintaining accurate records, and delivering regulatory training.
Location: College Station, Texas, United States; onsite staff position
Company
Texas A&M University supports ethical and compliant research involving human participants through its Human Research Protection Program.
What you will do
- Coordinate all aspects of Institutional Review Board (IRB) reviews according to institutional guidelines and federal regulations.
- Advise faculty, staff, and students on preparing protocol applications and conduct pre-reviews, including exempt-status determinations.
- Provide guidance on human-subjects research requirements and respond to compliance questions from investigators and committee members.
- Prepare IRB meeting materials, agendas, correspondence, minutes, and reports based on IRB determinations.
- Maintain accurate electronic and paper records and oversee data-entry quality for research submissions and related reports.
- Support regulatory training, outreach, and the development of HRPP processes and materials.
Requirements
- Bachelor’s degree in science, biomedical, health-related, or regulatory field.
- At least three years of experience in compliance, regulations, auditing, legal work, research, medical work, scientific writing, clinical trials, or a related area.
- Knowledge of federal human-subjects regulations, including HHS and FDA requirements.
- Analytical, organizational, communication, interpersonal, and multitasking skills.
- Ability to collaborate with interdisciplinary internal and external stakeholders.
- Working knowledge of Word, Excel, Adobe, and Access.
Nice to have
- Master’s degree in a health-related or regulatory field.
- Experience in human-subjects research compliance, social and behavioral research, biomedical research, or clinical trials management.
- Certified IRB Professional (CIP) or Certified Clinical Research Professional (CCRP) certification.
Culture & Benefits
- Medical, prescription, dental, vision, life, accidental death and dismemberment, flexible spending, and long-term disability insurance.
- Paid holidays, monthly sick leave, and paid vacation.
- Automatic enrollment in the Teacher Retirement System of Texas.
- Free exercise programs, wellness resources, LinkedIn Learning, and professional development support.
- Educational release time and tuition assistance for degree completion.
Hiring process
- A cover letter and resume are strongly recommended.
- Employment is contingent on credential verification and completion of a criminal history investigation because the position is security-sensitive.
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