[Hiring] Senior Clinical Research Associate @ICON plc

Role Description

As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Responsabilités:

• Surveiller les progrès des études cliniques aux centres d’étude ou à distance.
• Assurer que les études cliniques sont menées, documentées et signalées conformément au protocole, aux procédures opérationnelles normalisées (PON), aux bonnes pratiques cliniques (BPC) et à toutes les exigences réglementaires applicables.

Qualifications

• Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role.
• 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a level 3.
• ONCOLOGY MONITORING EXPERIENCE PREFERRED.
• ABILITY TO TRAVEL 70%.
• Knowledge of ICH and local regulatory authority regulations regarding drug trials.
• Applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status.

Benefits

• Competitive base salary and performance related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.
• Benefits may vary depending on role and location.