Clinical Scientist
Vor 5 Tagen
* Perform literature research
* Main deliverables include the clinical trial protocol and related documents
* Provides input for e.g. specifications, monitoring guidelines, data review manuals, ICF and CSRs
* Performs data review and medical monitoring during the conduct of the trial
* Provide scientific input into responses for IRBs/ECs and HAs
* Participates in discussions with stakeholders
* Coordinate the study committees
Qualifications* University degree (Master or PhD)
* Previous experience of working in clinical trial (scientist or monitor)
* At least 2 years experience
* Strong knowledge of ICH-GCP
* Knowledge of Phase I and II studies and cardiovascular TA exposure is of advantage
* Fluency in English (written and spoken)
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