Clinical Project Coordinator
Há 4 dias
Deliver quality services across various therapeutic indications.
We are seeking a Clinical Trial Administrator II to support clinical research projects by streamlining communication, maintaining systems, and managing documents and information.
Key Responsibilities:- Customize site ICF/patient documents for distribution to sites
- Prepare and submit EC-IRB documentation
- Maintain Site Room, Veeva Vault, electronic Trial Master File, and CTMs (including setup and maintenance)
- Prepare site files for SIV printing and assembly
- Collect and file site documents for MOH submissions
- Coordinate document translation
- Collect, review, and file site documents
- College/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
- Proficiency in English and Portuguese
- Ability to plan and work in a dynamic team environment
- Strong communication and collaboration skills
This role offers the opportunity to develop strong organizational and problem-solving skills, as well as a deep understanding of clinical trial operations.
As a key member of our team, you will be responsible for ensuring timely and accurate completion of tasks and meeting project deadlines.
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