(Senior) Clinical Trial Assistant
(Senior) Clinical Trial Assistant
Key Responsibilities
- Maintain and file essential clinical trial documents and completeness check of TMF
- Responsible for quality check of documents during filing
- General administrative tasks;
- Set up meetings;
- General assistance of the Clinical Operations team (onboarding of new Clinical Operations & Clinical Development team members, preparation of overviews and output, etc);
- Support in vendor and site agreement workflow
- Creation of purchase orders and reviewing of invoices for the Clinical Operations and Clinical Development team.
Skills, Knowledge and Expertise
- Advanced (e.g. Masters) degree or equivalent education / degree in life sciences;
- 2 – 3 years of experience in a similar role;
- Knowledge of ICH Good Clinical Practice (GCP)
- You master the English language;
- You have extensive experience with MS Office (in particular Word, Outlook, Excel and PowerPoint);
- You are a born organizer and thrive when given the opportunity to help others;
- You have a high level of quality and an eye for detail;
Please note that this role is an onsite/hybrid role and we will require candidates to be able to travel into the office. Candidates currently not living in the USA or at a reasonable travel distance from Cambridge, Massachusetts, will not be considered for the selection process.
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