IrvineFull TimeEngineering
Remotely
documentationstatisticsclinical data analysispkclinical protocolsdata presentationliterature search
Job Description
📋 Description
- Prepare scientific reports/presentations related to clinical trials using templates
- Coordinate advisory meeting agendas, slide decks, and consulting agreements
- Ensure compliance with IQS documents and study protocols
- Lead study development with current electronic document processes
- Handle task flow from function/MD staff within timelines
- Analyze clinical study data (PK, safety, efficacy) with available software
🎯 Requirements
- Bachelors/Master’s in science with 11+ years pharma experience, or Pharm-D/PhD with 1+ years
- Ability to understand complex clinical study principles
- Advanced data analysis and presentation/report generation skills
- Experience in team leadership or scientific project leadership
- Experience in clinical research, drug development, or therapeutic area operations
- Strong verbal and written communication skills
🎁 Benefits
- Comprehensive benefits including PTO, medical/dental/vision, 401(k)
- Eligible for short-term and long-term incentive programs
- Additional company-wide benefits and equal opportunity employer
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