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4 часа назад

Clinical Research Coordinator II - Annapolis/Columbia (Oncology)

51 545 - 88 987$
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
Clinical Research Coordinator II - Annapolis/Columbia (Oncology): Coordinating patient recruitment, enrollment, care, documentation, and protocol compliance for oncology clinical trials with an accent on informed consent, patient assessments, regulatory records, and research data. Focus on maintaining investigational drug accountability, preparing adverse event and IRB documentation, supporting audits, and improving research quality in an oncology clinic.

Location: Annapolis/Columbia, Maryland; full-time, on-site, Monday through Friday

Salary: $51,545–$88,987 per year

Company

Maryland Oncology Hematology provides cancer care through more than 15 locations across Maryland and Washington, DC.

What you will do

  • Screen, consent, and enroll patients in oncology clinical trials.
  • Coordinate patient visits and care according to study protocols, including investigational drug accountability and specimen shipments.
  • Assess and document patient condition changes, adverse events, concomitant medications, treatment response, and protocol compliance.
  • Prepare protocol worksheets, adverse event reports, IRB documents, continuing review reports, and other regulatory records.
  • Support monitoring and auditing visits, protocol activity reporting, accrual tracking, data entry compliance, and research financial reporting.
  • Educate clinic staff, contribute to action plans and process improvements, and help maintain research quality and SOP compliance.

Requirements

  • Associate’s degree in a clinical or scientific discipline required; bachelor’s degree preferred.
  • At least three years of experience in a clinical or scientific discipline required, preferably in oncology.
  • Experience with Microsoft Office and strong communication, organization, multitasking, time management, interpersonal, and attention-to-detail skills.
  • Extensive patient-facing experience and the ability to work independently in a fast-paced clinical environment.
  • Ability to perform basic clinical assessments and work with physicians and other healthcare providers.
  • Hazmat and/or IATA training is required for applicable specimen-shipping duties.

Nice to have

  • Bachelor’s degree in a clinical or scientific discipline.
  • SoCRA or ACRP certification.
  • Oncology, clinical research, and physician-collaboration experience.

Culture & Benefits

  • Supportive clinical research environment focused on patients, physicians, and colleagues.
  • Traditional office and oncology/hematology clinic setting.
  • Work includes computer-based duties, extended standing and walking, and occasional lifting of up to 40 pounds.
  • Reasonable accommodations are available for individuals with disabilities.

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