Clinical Research Associate II — Global Trials & Impact

KCR Placement

Center Square (PA)

Remoto

USD 70.000 - 100.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Descrizione del lavoro

ICON Strategic Solutions in the United States seeks a Clinical Research Associate II to design and monitor clinical trials, interpreting complex medical data and advancing innovative therapies.

As a CRA II, you will lead site qualification, initiation, monitoring, and close-out visits, ensure protocol compliance, data integrity, and patient safety, and collaborate with investigators and site staff to drive study success. Travel about 60% is expected.

Competenze

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

Mansioni

  • Conduct 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.

Conoscenze

Site monitoring
Travel readiness
ICH-GCP knowledge
Excellent communication
Independent work

Formazione

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

Descrizione del lavoro

ICON Strategic Solutions in the United States seeks a Clinical Research Associate II to design and monitor clinical trials, interpreting complex medical data and advancing innovative therapies.

As a CRA II, you will lead site qualification, initiation, monitoring, and close-out visits, ensure protocol compliance, data integrity, and patient safety, and collaborate with investigators and site staff to drive study success. Travel about 60% is expected.

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