Job Description
As a Study Support Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence
**What you will be doing**:
The Study Support Assistant will support administrative activities at sponsor's sites.
**Pre-screening and screening phase**:
- Support the submission of the protocol and other documents to the ethics committee (EC) for approval and the development and maintenance of files and binders.
**During trial conduct**:
- Assist with scheduling patient visits.
- Transcription of source document datapoints into EDC including query response according to the timelines and which can be clearly accessed in source documents.
- Submission of applicable trial documents to the ethical and regulatory entities.
- Archive and maintenance of the regulatory folders and binders.
- On-site and off-site monitoring visit support, such as communication with CRAs for scheduling visits, providing access ...
**What you will be doing**:
The Study Support Assistant will support administrative activities at sponsor's sites.
**Pre-screening and screening phase**:
- Support the submission of the protocol and other documents to the ethics committee (EC) for approval and the development and maintenance of files and binders.
**During trial conduct**:
- Assist with scheduling patient visits.
- Transcription of source document datapoints into EDC including query response according to the timelines and which can be clearly accessed in source documents.
- Submission of applicable trial documents to the ethical and regulatory entities.
- Archive and maintenance of the regulatory folders and binders.
- On-site and off-site monitoring visit support, such as communication with CRAs for scheduling visits, providing access ...
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