Oncology Clinical Research Associate – Site Monitoring

ICON Strategic Solutions

Pennsylvania

On-site

USD 65,000 - 95,000

Full time

7 days ago
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Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate – Oncology to monitor trials across OH, PA and VA, ensuring patient safety, data integrity and protocol compliance. You will conduct site qualification, initiation, monitoring and close-out visits and collaborate with investigators to drive study success.

The role requires oncology monitoring experience, ICH-GCP knowledge, and travel up to 60-75% within the Northeast region. A scientific or healthcare-related degree is required.

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

Attention to detail
Organizational skills
Communication skills
Independent and collaborative work
Travel readiness up to 60-75%

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate – Oncology to monitor trials across OH, PA and VA, ensuring patient safety, data integrity and protocol compliance. You will conduct site qualification, initiation, monitoring and close-out visits and collaborate with investigators to drive study success.

The role requires oncology monitoring experience, ICH-GCP knowledge, and travel up to 60-75% within the Northeast region. A scientific or healthcare-related degree is required.

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