Senior CRA - Oncology Trials | Regional Travel (Midwest)

Worldwide; Illinois; Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials in the United States is seeking a Clinical Research Associate to oversee site activities within oncology trials across multiple sites, with emphasis on regulatory and data integrity.

You will work with study teams, manage TMF and site start-up tasks, and travel regionally to support study milestones; 5+ years CRA, degree, oncology required, Midwest/Central region, strong communication, and proficiency in MS Office/CTMS/EDC.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Oncology is required.
• Candidates must reside in the Midwest or Central Regions.
• Willingness to travel regionally required.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of the clinical study, including site identification, start-up activities, regulatory documents, contracts/budgets, data collection and safety reporting, site maintenance, and study close-out.

Skills

Interpersonal communication

Organizational skills

Independent work

Education

Bachelor's degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials in the United States is seeking a Clinical Research Associate to oversee site activities within oncology trials across multiple sites, with emphasis on regulatory and data integrity.

You will work with study teams, manage TMF and site start-up tasks, and travel regionally to support study milestones; 5+ years CRA, degree, oncology required, Midwest/Central region, strong communication, and proficiency in MS Office/CTMS/EDC.