Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.
Only CVs in English will be accepted.
You will be responsible for:
- Customization of Site ICF/patient documents before sending it to sites;
- EC- IRB submissions;
- Site Room, Veeva Vault, electronic Trial Master file and CTMs (including set up and maintenance);
- Site file preparation for SIV (Printing and assembling documents);
- Collection and filing documents from sites for MOH submissions;
- Coordinate the translation of documents;
- Collection/QC/filing of site documents– all documents required per Data Management Plan, not limited to Investigational Product Release-Enabling Document;
- Accesses to systems: Collecting vendor access information from sites in the format requested.
#LI-Hybrid
- College/University degree or an equivalent combination of education, training & experience;
- Minimum 1 year of industry experience
- Administrative work experience, preferably in an international setting;
- Local regulations knowledge;
- Prior experience in Clinical Research;
- Full working proficiency in English and Portuguese;
- Proficiency in MS Office applications;
- Ability to plan and work in a dynamic team environment;
- Communication and collaboration skills.
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
