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ROLE SUMMARY
The successful candidate will collaborate with study teams working effectively within the clinical triad (clinician clinical pharmacologist and statistician) to design studies develop protocols write statistical analysis plans perform statistical analysis write reports present results summarizing findings and develop publications of results. Successful candidate would also participate in regulatory submissions and response to regulatory queries. The candidate will directly contribute to Company success by increasing the strength of study designs interpretability of results regulatory strategy interactions biomarker strategies and by implementing methods of model informed drug development.
ROLE RESPONSIBILITIES
BASIC QUALIFICATIONS
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Remote Work :
No
Full Time