Clinical Trial Supply Specialist
1 mese fa
Job Summary:
We are seeking an experienced Clinical Trial Supply Specialist to join our team at IQVIA. The successful candidate will be responsible for reviewing eTMF plans, uploading documents, and performing quality control of the eTMF.
Key Responsibilities:
- Review eTMF plans and ensure compliance with regulatory requirements
- Upload documents to the eTMF and perform ongoing quality control
- Monitor eTMF quality issues and follow up with relevant functions
- Provide support to eTMF users on the use of the system
- Archive study CTS related documentation in the Company CTS repository
Requirements and Skills:
- High School and/or College Degree
- Significant experience in a similar job in the industry or CRO
- Solid knowledge of clinical data management
- Problem-solving skills
- Proficient in English
Working Environment:
This is a maternity replacement position, and the successful candidate will be working in a dynamic and exciting environment.
IQVIA reserves the right to evaluate candidates with domicile/residence and work experience/study with requirements responding to the open request.
Applications without the requirements will not be fully taken into account.
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