data analysishipaaclinical researchclinical trialsfda regulationselectronic medical recordsgood clinical practiceelectronic data capturehuman subject protection
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$45к/год
$73к$93кмедиана$110к
По похожим ролям (50) ~ $93к/год
Прикинули из $3.8к/мес × 12
38
Не очень вакансия
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Зарплата заметно ниже рыночного ориентира, а в роли объединены клинические исследования, работа с участниками, анализ данных, регуляторная документация, закупки и обучение сотрудников. Грантовое финансирование и возможная работа вне обычных часов добавляют неопределенности, поэтому льготы могут не компенсировать низкую оплату и широкий круг задач.
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Оплата ниже рынкаМного разных задачЗависимость от грантаРабота вне графикаХороший соцпакетКлинические исследования
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Research Specialist I (Clinical Research): Compiling and analyzing clinical research data, managing study documentation, specimens, participant visits, and protocol compliance with an accent on clinical trial operations, regulatory requirements, and human subject protections. Focus on maintaining electronic research databases, supporting audits and monitoring visits, screening and recruiting participants, and coordinating research materials and supplies.
Location: Corpus Christi, Texas; the employee will work at a private clinical office in Corpus Christi and report to IBT in downtown Houston, Texas. Weekend and after-hours work may be required, with travel as needed.
Salary: $3,750 per month.
Company
Texas A&M Health is an academic health center comprising colleges, centers, and institutes focused on health education, research, and team-based healthcare delivery.
What you will do
Compile, review, summarize, and analyze clinical research data and metadata; compute projections and perform tests.
Collect samples and scientific 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 HIPAA compliance and participant confidentiality.
Prepare study materials, regulatory binders, research records, and documentation for sponsor monitoring visits, audits, and inspections.
Support research publications, funding proposals, project financial accounts, laboratory purchasing, inventory tracking, and staff training.
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, human subject protections, and research protocols.
Proficiency with Microsoft Office, databases, electronic medical record systems, and applicable computer software.
Ability to multitask, organize work, communicate effectively, collaborate, and maintain attention to detail.
Ability to work onsite in Corpus Christi, Texas, including possible weekends and after-hours.
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, dental, vision, life, accidental death and dismemberment, flexible spending, and long-term disability insurance.
Texas A&M contributions toward employee health and basic life insurance premiums.
Paid holidays, monthly paid sick leave, and paid vacation.
Automatic enrollment in the Teacher Retirement System of Texas.
Professional development through LinkedIn Learning, webinars, conference support, educational release time, and tuition assistance.
Health and wellness programs, including free exercise programs and release time.
Hiring process
Submit complete application data or attach a complete resume.
Employment is contingent on credential verification and completion of a criminal history investigation.
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