CRA II — Ophthalmology Trials | Travel‑Ready

ICON Strategic Solutions

Pennsylvania

Vor Ort

USD 70.000 - 90.000

Vollzeit

vor 5 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Health insurance
Competitive retirement planning
Global Employee Assistance Program

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Research Associate (CRA II) in the Northeast region. You will design and analyze clinical trials, interpreting complex medical data and contributing to trials across Ophthalmology or multi-TA indications.

You will conduct site visits, ensure patient safety and data integrity, and collaborate with investigators to ensure smooth study conduct. Travel approximately 60% is required.

Qualifikationen

  • Bachelor's degree in a scientific or healthcare-related field is required.
  • Minimum of 2 years experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Willingness to travel approximately 60% of the time.

Aufgaben

  • Conduct site qualification, initiation, monitoring, and close-out visits.
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborate with investigators and site staff to facilitate study conduct.
  • Perform data review and resolve queries to maintain high-quality data.
  • Contribute to the preparation and review of study documentation, including protocols and CSRs.

Kenntnisse

Clinical trial monitoring
Independent work
Collaborative team player
Strong communication

Ausbildung

Bachelor's degree in science or healthcare

Jobbeschreibung

ICON Strategic Solutions is seeking a Clinical Research Associate (CRA II) in the Northeast region. You will design and analyze clinical trials, interpreting complex medical data and contributing to trials across Ophthalmology or multi-TA indications.

You will conduct site visits, ensure patient safety and data integrity, and collaborate with investigators to ensure smooth study conduct. Travel approximately 60% is required.

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