We are looking for a Senior Clinical Research Associate (Level I) to support clinical trial monitoring and site management. You will ensure protocol and regulatory compliance, manage documentation, and collaborate with investigational sites. Ideal candidates have experience in clinical research, particularly in Oncology and Cell Therapy.
Skills
- clinical monitoring
- ich-gcp compliance
- oncology clinical research
- risk based monitoring
- cell therapy clinical research
- sdr
- sdv
- crf review
- root cause analysis
- clinical trial management system
- site management
- regulatory compliance
- investigational product assessment
- trial close out
- investigator site initiation
- essential document management
- clinical trial documentation
- project status reporting
- process improvement
- clinical research monitoring
- investigator identification
- clinical trial site review
- clinical trial site initiation
- clinical trial site retrieval
- clinical trial site management
