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23 часа назад

Research Specialist I (Clinical Research)

3 750$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Research Specialist I (Clinical Research): Compiling and analyzing clinical research data, collecting specimens and measurements, and supporting clinical trial operations with an accent on protocol compliance, participant confidentiality, and regulatory documentation. Focus on screening and scheduling participants, maintaining electronic research records, preparing for audits, and executing protocols under FDA, IRB, and sponsor requirements.

Location: Corpus Christi, Texas; work is performed at a non-Texas A&M private clinical office, with reporting to the IBT location in downtown Houston. Weekend and after-hours work may be required, and travel may be necessary.

Salary: $3,750 per month minimum.

Company

Texas A&M Health is an academic health center comprising colleges, centers, and institutes focused on health education, innovative 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, measurements, and research specimens, including processing, shipping, and tracking.
  • Maintain clinical trial data collection, enrollment, follow-up, protocol compliance, research records, regulatory binders, and study documentation.
  • Screen participants, schedule study visits, and support participant recruitment and retention.
  • Enter study data into electronic databases and EMR systems and prepare summarized results for scientific or client-focused publications.
  • Support sponsor monitoring visits, audits, inspections, purchasing, grant invoice processing, and research 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, and human subject protections.
  • Proficiency with Microsoft Office, databases, electronic medical record systems, and applicable computer software.
  • Ability to multitask, collaborate, organize work, communicate effectively, and use laboratory or technical equipment.

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, equivalent certification, or the ability to obtain it after hire.

Culture & Benefits

  • Medical, prescription drug, dental, vision, life, accidental death and dismemberment, 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, LinkedIn Learning, webinars, and limited professional development support.
  • Educational release time and tuition assistance for degree completion.

Hiring process

  • Applications must include complete application data or a complete resume.
  • Employment is contingent on credential verification, institutional checks, and a criminal history investigation.

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