Join Parexel's clinical team as a Clinical Research Associate II, overseeing research sites and enhancing patient safety in clinical trials. This role involves significant site interaction and travel.

The Clinical Research Associate II role requires effective management and monitoring of clinical trial sites. You will engage with site personnel to ensure compliance with protocols and provide training to safeguard patient welfare. Your expertise will help maintain the integrity of the trial and address any site-related issues promptly.

Key Responsibilities:
• Ensure adherence to Study Monitoring Plans and GCP
• Collaborate with Site Care Partner for site training
• Resolve protocol-related issues and implement corrective actions




• Conduct onsite and remote monitoring activities
• Oversee investigational product management at sites

Requirements:
• At least 2 years of relevant monitoring experience
• Bachelor’s degree in a life sciences field
• Robust English proficiency and local language skills
• Ability to travel extensively (60-80%)
• Required valid driver’s license and passport

Bring your expertise in clinical trials and make a difference in patient safety with Parexel.
#J-18808-Ljbffr

📌 Clinical Research Associate II Position (Newfoundland and Labrador)
🏢 Parexel
📍 Newfoundland and Labrador