Real World Evidence Contractor (Biopharma)

TL;DR

Real World Evidence Contractor (Biopharma): Supporting real-world evidence (RWE) research efforts by designing and executing studies with an accent on literature reviews and large healthcare dataset analysis. Focus on generating insights for regulatory, clinical, and commercial objectives while ensuring scientific rigor.

Location: Hybrid position based in Cary, NC. Open to remote candidates, with a high preference for ET/CT time zone location.

Company

An international research-focused biopharmaceutical group with 90 years of experience operating in 31 countries.

What you will do

• Assist in the design and execution of RWE studies, including literature reviews, data analysis, and interpretation of findings.
• Analyze large healthcare datasets to generate insights that support regulatory, clinical, and commercial objectives.
• Summarize and communicate findings through reports, presentations, and publications.
• Collaborate with internal teams, external partners, and vendors to advance project goals.
• Stay current with real-world data methodologies and regulatory considerations.

Requirements

• PhD in epidemiology, health outcomes research, or a related field.
• Strong analytical skills with exposure to RWE methodologies and study design.
• Proficiency in statistical programming (R, SAS, or Python) and experience with healthcare data.
• Strong communication skills, including scientific writing and presenting research findings.
• Ability to work independently and manage time effectively.
• Availability for at least 30 hours per week (1-year contract).

Culture & Benefits

• Comprehensive healthcare programs.
• Work-life balance initiatives.
• Robust relocation support.
• Competitive salary package with performance bonuses.
• Flexible working arrangements and remote work options.