To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.
Responsibilities
- 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.