Clinical Research Associate Pipeline
Novo Nordisk
- Roma
- Tempo indeterminato
- Full time
- Primary point of contact between site staff and Novo Nordisk, act as a site manager and an ambassador for the company and contributes to making Novo Nordisk the preferred partner in clinical trials.
- Overall site management, including site monitoring and remote monitoring as applicable
- Ensure that trial site staff are properly trained to conduct the trial(s), provide necessary training, and identify and flag any development areas and implement mitigations.
- Managing trial sites to meet patient recruitment and retention target, aimed at successful completion of the clinical programme.
- Contribute to or lead selection of sites, in collaboration with CDC and local colleagues such as Line Managers and Medical Affairs.
- You also meet the following requirements:
- You are Fluent in both Italian and English.
- Knowledge of clinical trial methodology
- Knowledge of the clinical trials environment – ICH GCP, regulatory issues, SOPs
- Good working knowledge of electronic clinical trials systems – CTMS, EDC, IWRS, electronic TMF
- Basic GCP qualification