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POST DATE 9/15/2016
END DATE 10/14/2016
East Hanover, NJ
JOB DESCRIPTIONJob Description:
OVERVIEWUtilizing CSRs, prepare results from a number of therapeutic areas, in the Clinical Trial Results format, for submission to the EMA's results website,EudraCT.Circulate the prepared results for review by key clinical team members, addressing team questions, archiving the approvals and prepared result into the document repository.Prepare and make the submission in EudraCT. Assist the clinical disclosure team with any other support required for meeting the EU backlog of results submission to EudraCT or in facilitating clinical team review of redacted CSRs for voluntary data sharing. Skills: Must have a minimum of 10 years clinical research and development experience, preparation of writing protocols, interpreting trial results and preparation ofCSRs.Ability to influence and successfully work within complex cross divisional matrix across different cultures.Strong negotiation and conflict resolution skills;well organized, strong planning, tracking, problem solving and decision making skills. Education: Minimum Bachelor degree in a scientific discipline preferred.
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