Senior Clinical Research Associate I (FSP)

We are looking for a Senior Clinical Research Associate I to coordinate and monitor clinical trial sites, ensuring compliance with protocols and regulations. The role involves site management, data accuracy, and collaboration with investigational sites. Ideal for candidates with clinical research monitoring experience and a background in life sciences or nursing.

Skills

• clinical monitoring
• ich-gcp compliance
• bachelor's degree in life sciences
• risk based monitoring
• root cause analysis
• clinical trial management systems
• regulatory documentation
• site management
• sdr
• sdv
• crf review
• investigator site initiation
• trial close out
• audit readiness
• medical terminology
• clinical research monitoring
• business writing
• investigator identification
• process improvement
• project team collaboration
• presentation skills
• organizational skills