Consultant – Recherche quantitative ou mixte centrée sur le patient – Quantitative or Mixed Methods Patient-Centered Research
| Company | IQVIA |
|---|---|
| Location | Pointe-Claire, QC, Canada, Ottawa, ON, Canada |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Master’s, PhD |
| Experience Level | Senior, Expert or higher |
Requirements
- PhD + scientific consulting experience within the pharmaceutical industry strongly preferred
- PhD + postdoc preferred
- Master’s degree + at least 4 years of experience in scientific pharma consulting acceptable
- Experience in survey research/measurement, quantitative research methods, and literature search methods required
- Three years of SAS or similar statistical programming experience is required
- Proficient in MS Office (Word, Excel, PowerPoint)
- Experience with bibliographic software, such as Citavi
- At least 5 abstracts accepted for presentation at a major scientific venue, or equivalent experience teaching college-level curriculum or industry workshops
- At least 1 peer-reviewed published article or equivalent experience
- Familiarity with regulatory guidance and current developments in the pharmaceutical and healthcare industries
- Fluency in English
Responsibilities
- Supports and assists research teams with study design, literature reviews, development of study materials, data management and analysis, and quality assurance
- Independently performs statistical programming and statistical analyses according to a statistical analysis plan, and develops required graphs, tables, and figures using the appropriate software tools
- Co-authors technical reports, summaries, manuscripts, posters, and presentations
- Prepares for and presents at professional meetings and client-sponsored events
- Proactively problem solves; identifies and helps drive resolution of issues at all phases of the project that could affect success
- Interacts effectively and collegially with all employees, fostering a supportive and cross departmental sharing environment
Preferred Qualifications
- Experience with FDA PRO guidance is a plus