Offer summary
Qualifications:
Minimum 2 years of experience as a Clinical Research Associate, Experience in Pharma, CRO, or Biotech, Good understanding of Clinical Study Management, Bachelor’s degree in life science or equivalent, Strong oncology experience.
Key responsabilities:
- Local responsibility for study delivery at allocated sites
- Work with Monitors and Local Study Team to meet commitments
- Primary contact for study site management
- Preparation, initiation, monitoring, and closure of clinical centers
- Ensure compliance with ICH, GCP, and local regulations