Senior Oncology Clinical Research Coordinator (Hybrid)

John Hopkin’s University; Baltimore (MD); Hybrid; USD 42,000 - 74,000; Full time

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