Senior Clinical Research Associate

Join us as a Senior Clinical Research Associate and play a key role in monitoring clinical trials, ensuring protocol and regulatory compliance. You will manage site processes, conduct site visits, and support data integrity. Ideal candidates bring experience in clinical research monitoring and strong communication skills.

Skills

• clinical monitoring
• ich-gcp compliance
• risk based monitoring
• sdr
• sdv
• crf review
• root cause analysis
• clinical trial management system
• site management
• regulatory compliance
• problem solving
• critical thinking
• investigational product assessment
• trial close out
• essential document management
• medical terminology
• clinical research monitoring
• project status reporting
• investigator site initiation
• business writing
• presentation skills
• team collaboration