- Saint-Maur-des-Fossés, Île-de-France, France
- Hybrid
- Full-time · Entry
- 1+ years
Provide operational support for clinical study startup processes in France.
Responsibilities
- Support site identification and selection process
- Collect and review documents for ethics and regulatory review and approval
- Prepare packages of site documents for drug release to clinical sites
- Prepare and negotiate site contracts and budgets
- Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters till the moment of site activation
Requirements
- College/University degree or an equivalent combination of education, training and experience