Senior Oncology Clinical Research Coordinator (Hybrid)

The Johns Hopkins University

Baltimore (MD)

Hybrid

USD 42,000 - 74,000

Full time

14 days+
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Job summary

The Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities of multiple clinical studies at two sites, including inpatient and translational research components.

You will assist in feasibility assessments, protocol development, and sponsor communications, ensuring compliance and robust data systems. Responsibilities include developing SOPs, consent forms, and IRB submissions, maintaining regulatory files, budgeting input, and leading participant

Qualifications

  • Bachelor's Degree in a related field.
  • Three years of related experience.
  • Experience with IRB and regulatory compliance is a plus.

Responsibilities

  • Oversee day-to-day activities of multiple clinical studies across two sites.
  • Develop SOPs and data collection forms from protocols.
  • Create consent forms for clinical trials based on protocols.
  • Prepare material for IRB submissions and maintain regulatory files.
  • Collaborate with sponsors to assess resources and costs.
  • Ensure compliance with all protocols and regulations.
  • Assist in budget development and recruitment strategy for participants.
  • Set up data collection systems and manage study data.
  • Conduct data quality checks and site audits.
  • Provide status updates and suggest protocol improvements.

Skills

Clinical research coordination
IRB knowledge

Education

Bachelor's Degree

Job description

The Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities of multiple clinical studies at two sites, including inpatient and translational research components.

You will assist in feasibility assessments, protocol development, and sponsor communications, ensuring compliance and robust data systems. Responsibilities include developing SOPs, consent forms, and IRB submissions, maintaining regulatory files, budgeting input, and leading participant

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