Senior Clinical Operations Coordinator
Há 3 dias
At PSI Cro, we offer a dynamic and innovative work environment where you can advance your career in clinical research. As a Clinical Trial Administrator Ii, you will play a key role in streamlining communication, maintaining systems, and managing documents and information for our international team.
Responsibilities- Customize Site ICF/patient documents before sending them to sites;
- Submit EC-IRB documents;
- Maintain Site Room, Veeva Vault, electronic Trial Master file, and CTMs (including setup and maintenance);
- Prepare Site files for SIV (Printing and assembling documents);
- Collect and file documents from sites for MOH submissions;
- Coordinate document translations;
- Collect, quality-check, and file site documents;
- Ensure compliance with Data Management Plans, including Investigational Product Release-Enabling Document;
- Access systems: Collect vendor access information from sites in the requested format.
- College or University degree or equivalent combination of education, training, and experience;
- Minimum 1 year of industry experience;
- Administrative work experience, preferably in an international setting;
- Knowledge of local regulations;
- Prior experience in Clinical Research;
- Full working proficiency in English and Portuguese;
- Ability to plan and work in a dynamic team environment;
- Strong communication and collaboration skills.
We offer a competitive salary range of $60,000 - $80,000 per annum, depending on experience. Additional benefits include opportunities for professional growth, a dynamic work environment, and a chance to work with a leading Contract Research Organization. Advance your career in clinical research with us
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