Director leading observational studies in pharmaceutical consulting at RTI Health Solutions. Overseeing research integrity, project management, and client engagement for high-impact projects.
Responsibilities
Champion scientific integrity and excellence through robust analytical approaches, evidence-based decision-making, and a commitment to maintaining the highest standards of research quality.
Provides thought leadership with recognized expertise and industry influence.
Lead and oversee complex, multi-country site-based and cross-sectional observational studies, including primary data collection initiatives.
Develop protocols, survey instruments, data collection plans, analysis strategies, and high-quality deliverables (reports, manuscripts, slide decks).
Serve as a senior reviewer or lead for proposals, protocols, analysis plans, and deliverables, ensuring methodological rigor, consistency, and quality.
Requirements
Master’s degree or higher (e.g., MPH, MS, PharmD, PhD, MD, RN/PA) with 8+ years of relevant experience in pharmaceutical, biotechnology, medical device, epidemiology, or HEOR/RWE consulting.
Experience designing and executing primary data collection and observational RWE studies, including survey methodology and instrument development.
Demonstrated experience leading projects, mentoring staff, and contributing to scientific deliverables.
Experience in successfully managing a cross-functional team.
Familiarity with ethics and privacy regulations, patient recruitment strategies, data management systems, and mixed-method research approaches.
Benefits
Comprehensive healthcare coverage
Retirement savings plan with employer matching contributions
Paid time off including vacation and sick days
Professional training and development opportunities
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