Offer summary
Qualifications:
At least 5 years' industry experience, At least 3 years leading multi-site clinical trials, B.Sc. in a related field of study, Strong knowledge of GCP and ICH standards, Fluency in English; bilingualism is an asset.Key responsabilities:
- Serve as primary contact for stakeholders
- Ensure studies are 'audit ready' at all times
- Manage operational aspects of the trial
- Lead study start-up process & quality assurance
- Monitor and report on recruitment status