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5 дней назад

Data Coordinator (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle/senior
Английский
b2
Страна
US
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Описание вакансии

Текст:
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TL;DR
Data Coordinator (Clinical Research) (Oncology): Collecting, coordinating, processing, and quality-controlling clinical trial data for oncology research with an accent on regulatory compliance, accurate case report forms, and confidential research records. Focus on resolving data queries, supporting sponsor audits, maintaining protocol documentation, and coordinating specimens, imaging, and patient follow-up activities.

Location: Austin, Texas, United States; support for the South Austin location

Company

Texas Oncology is a large community oncology provider delivering cancer care and conducting oncology research across Texas and southeastern Oklahoma.

What you will do

  • Collect, coordinate, process, and quality-control clinical trial data.
  • Extract patient-visit data into case report forms and submit it according to research procedures and timelines.
  • Resolve data queries and communicate data concerns with clinical staff and research management.
  • Maintain clinical trial management system records, patient tracking functions, research files, and confidential documentation.
  • Participate in sponsor monitoring and audit visits while ensuring data and queries meet research and sponsor requirements.
  • Support research supply management, patient follow-up scheduling, and the collection and processing of specimens and imaging documents.

Requirements

  • High school diploma required; an associate degree is strongly desired and a bachelor's degree is preferred.
  • Level 1: 0–3 years of work experience and some medical office experience, preferably in oncology.
  • Level 2: At least 3 years of medical office experience and 3 years of Data Coordinator experience.
  • Senior level: At least 7 years of Data Coordinator experience and medical terminology knowledge.
  • Work must be performed in a traditional oncology and hematology clinic environment, including standing, walking, patient handling, and occasional lifting of up to 40 pounds.
  • Compliance with US Oncology Research procedures, Good Clinical Practice, HIPAA, and applicable regulations is required.

Nice to have

  • SoCRA or ACRP certification.
  • Previous oncology medical office experience.

Culture & Benefits

  • Full-time Monday–Friday schedule from 8:30 a.m. to 5:00 p.m.
  • No weekends, on-call shifts, or major holidays.
  • Collaborative and supportive work environment.
  • Medical, dental, vision, life, short-term and long-term disability coverage.
  • Generous paid time off, 401(k) with company match, wellness program, tuition reimbursement, employee assistance program, and retailer discounts.

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