Clinical Research Associate Pipeline
Novo Nordisk
- Roma
- Tempo indeterminato
- Full time
Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...Category×Select how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Clinical Research Associate PipelineCategory: Clinical DevelopmentLocation:Roma, Lazio, ITJoining the CRA PipelineBy applying for the pipeline, you will be considered as a potential match for CRA positions, which align with your background, skills and interests. We'll match your profile proactively to ensure you don't miss out on a life-changing career.We'll match your profile proactively with relevant positions. Once a Hiring Manager shows interest in your profile, our Recruitment team will reach out to you and tell you more about the current position and invite you for the 1st Interview.You will remain a part of the Pipeline for up to 6 months unless you withdraw your application. We kindly ask you to inform us or withdraw your application, if you get a new job, which will ensure fair recruitment process to everyone and spare you for us contacting you.The pipeline is open for applications due to GDPR we close the pipelines after 6 months and send email notifications to all active candidates when they are closed, with a link to where you can re-apply to our new CRA Pipeline.The PositionThe CRA is responsible for managing clinical trial sites at every stage of the clinical trial process in accordance with the Company's policies and procedures, relevant legislation, and ICH GCP requirements, whilst maintaining the standards of the Novo Nordisk Way.Main accountabilities of the role:
- 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