Oncology Clinical Research Associate – Travel‑Ready & Impact

ICON Strategic Solutions

California (MO)

On-site

USD 91,000 - 114,000

Full time

8 days ago
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Benefits offered by this job

Health insurance
Retirement planning opportunities
Employee Assistance Programme

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate specializing in HemOnc to support California or Colorado sites within a sponsor-dedicated model. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity and patient safety.

Travel up to 60-75% is expected. Requirements include a Bachelor's degree in a scientific/healthcare field, 2+ years of CRA experience with oncology monitoring, and strong organizational

Qualifications

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • Oncology monitoring experience required.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Clinical trial monitoring
ICH-GCP knowledge
Regulatory understanding
Attention to detail
Communication skills

Education

Bachelor's degree in scientific or healthcare field

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate specializing in HemOnc to support California or Colorado sites within a sponsor-dedicated model. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity and patient safety.

Travel up to 60-75% is expected. Requirements include a Bachelor's degree in a scientific/healthcare field, 2+ years of CRA experience with oncology monitoring, and strong organizational

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