Hematologic Oncology Clinical Trials Coordinator

Allegheny Health Network

Pittsburgh (Allegheny County)

On-site

USD 55,000 - 85,000

Full time

14 days+

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Job summary

Allegheny Health Network seeks a clinical research professional to plan, coordinate, and manage initiation to completion of trials sponsored by internal and external entities. The role emphasizes regulatory compliance and maintaining study documentation.

Ideal candidates have an associate’s degree or RN, 1–3 years of experience, and prefer a Bachelor’s degree with certifications from ACRP or SOCRA. A driver's license may be required depending on facility needs, with Oncology research experience

Qualifications

  • Associate's degree, RN, or equivalent research experience.
  • 1-3 years' related experience.
  • Bachelor's Degree.
  • ACRP certification (CCRC) or SOCRA certification (CCRP) or ACRP-CP.
  • Driver's license may be required depending on facility requirements.
  • Experience in Hematologic Oncology Research.

Responsibilities

  • Identify patients eligible for clinical trials and provide in-service education to hospital staff involved in the investigational study.
  • Educate patients and families about investigational studies and participation requirements; obtain informed consent and monitor per protocol.
  • Collect, maintain, and store clinical data, case report forms, and regulatory binders per sponsor and regulatory bodies.
  • Plan, coordinate, and manage all activities for specific trials, ensuring patient safety and regulatory compliance.
  • Perform other duties as assigned or required.

Skills

Regulatory compliance
Documentation management

Education

Associate's degree
RN or equivalent research experience
Bachelor's Degree
ACRP/SOCRA certifications (CCRC/ACRP-CP/CCRP)
Hematologic Oncology Research experience

Job description

Allegheny Health Network seeks a clinical research professional to plan, coordinate, and manage initiation to completion of trials sponsored by internal and external entities. The role emphasizes regulatory compliance and maintaining study documentation.

Ideal candidates have an associate’s degree or RN, 1–3 years of experience, and prefer a Bachelor’s degree with certifications from ACRP or SOCRA. A driver's license may be required depending on facility needs, with Oncology research experience

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