2 дня назад
Research Specialist I (Clinical Research)
3 750$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Research Specialist I (Clinical Research): Supporting clinical research activities through data compilation, clinical trial tracking, participant screening, specimen processing, and protocol compliance with an accent on clinical data management, regulatory documentation, and human subject protections. Focus on analyzing clinical trial data, coordinating participant visits, maintaining HIPAA-compliant records, and preparing research materials for audits and publications.
Location: Houston, Texas; the position reports to IBT in downtown Houston, with the employee located at a private clinical office in Corpus Christi, Texas. On-site work may include weekends, work outside normal hours, and travel as required.
Salary: $3,750 per month minimum.
Company
Texas A&M Health is an academic health center supporting transformative education, innovative research, and team-based healthcare delivery.
What you will do
- Compile, review, summarize, and analyze clinical research data and metadata, including projections, tests, observations, and scientific measurements.
- Collect samples and measurements, process and track research specimens, and maintain clinical trial data collection systems.
- Support participant screening, recruitment, retention, scheduling, enrollment tracking, follow-up, and protocol compliance.
- Enter study data into electronic databases and EMR systems while maintaining participant confidentiality and HIPAA compliance.
- Maintain regulatory binders, research records, study documentation, participant materials, and training materials.
- Support sponsor monitoring visits, audits, inspections, publications, proposals, purchasing, inventory tracking, and grant invoice processing.
Requirements
- Bachelor’s degree or an equivalent combination of education and experience.
- Four years of related experience in a specialized and relevant research field.
- Knowledge of FDA regulations, Good Clinical Practice, HIPAA, and human subject protections.
- Proficient computer skills, including Microsoft Office Suite, databases, and electronic medical record systems.
- Ability to multitask, communicate effectively, organize work, maintain attention to detail, and collaborate with research personnel.
- Familiarity with laboratory or technical equipment and the ability to work on-site, including occasional weekends or after-hours work.
Nice to have
- Experience in a physician practice, hospital, oncology clinic, or other healthcare environment.
- Experience with electronic data capture systems and regulatory documentation.
- Current CITI Human Subjects Protection training certification or the ability to obtain it after hire.
Culture & Benefits
- Medical, prescription drug, dental, vision, life, AD&D, flexible spending, and long-term disability insurance.
- Paid annual holidays, monthly sick leave, and paid vacation.
- Automatic enrollment in the Teacher Retirement System of Texas.
- Free exercise programs, wellness resources, and professional development through LinkedIn Learning, webinars, and conference support.
- Educational release time and tuition assistance for degree completion.
- Grant-funded position; continued employment may depend on future funding.
Hiring process
- Applications must include complete application data or a complete resume.
- Employment is contingent upon credential verification and a criminal history investigation.
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