Clinical Research Associate - Site Management

Oversee clinical study delivery as a Clinical Research Associate. Ensure compliance and monitor site performance while collaborating with study teams for effective execution.

In this role, you will manage local clinical studies, ensuring adherence to timelines and protocols. With a focus on monitoring activities, you will identify and resolve study-related issues while training site personnel in relevant guidelines. Collaborating with cross-functional teams enhances successful site management and recruitment efforts.

Key Responsibilities:

• Perform site selection and monitoring visits
• Drive performance and timely resolutions of study issues
• Train and support Investigators and site staff
• Develop recruitment strategies and manage enrollment
• Prepare monitoring visit reports and documentation

Requirements

• Minimum 1 year CRA monitoring experience
• Bachelor’s degree in life science or related field
• Strong knowledge of ICH-GCP guidelines
• Excellent communication and collaboration skills
• Flexibility to travel up to 70% of the time

Enhance clinical research efforts by ensuring high-quality site management and compliance through effective collaboration.

#J-18808-Ljbffr