Prepare scientific reports and presentations related to clinical trials using available software and templates.
Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
Comply with procedures set forth in relevant IQS documents and Study protocols
Comply with the directives issued by the management regarding clinical studies.
Commit to producing work of the highest quality
Pay close attention to detail
Perform literature and competitive intelligence searches
Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis
Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.

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Associate I, Clinical Pharmacology Scientific Support & Reporting

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