Associate Director – Biostatistics

🔥 42 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $110k - $130k / year

⏰ Full Time

🟠 Senior

👔 Director

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RTI International

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1958

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

RTI International is an independent nonprofit research institute dedicated to improving the human condition through science-based solutions in climate, education, health, and equity. The institute engages in multidisciplinary research spanning diverse areas such as health care, international development, environmental sciences, and social and economic justice. RTI International collaborates with a wide range of partners including governments, businesses, universities, and non-profit organizations to conduct research and provide technical services. It aims to impact global wellbeing by leveraging expertise in fields such as climate change solutions, education reform, public health, food security, and more. RTI International also emphasizes corporate responsibility, sustainability, and commitment to quality and ethics in its operations.

📋 Description

• Perform statistical research tasks of moderate to high technical complexity, focusing on patient-reported outcomes and other clinical outcome assessments in clinical trials and real-world data • Plan, conduct, and document statistical analyses for clinical trials and observational studies • Develop simple to moderately complex statistical analysis plans and contribute to more complex SAPs under supervision • Write statistical sections of study reports, protocols, and proposals • Ensure the quality, accuracy, and timeliness of statistical analyses and programming outputs • Provide statistical and methodological solutions to internal, cross-functional project teams • Mentor and oversee less experienced staff on selected project tasks • Learn and apply new statistical methods in response to evolving project and research needs • Contribute to the scientific reputation and professional development of the biostatistics group • Prepare presentations for external audiences • Lead proposal development under limited supervision while collaborating closely with multidisciplinary project teams

🎯 Requirements

• Master's degree and at least 6 years of experience, PhD and at least 1 years of experience, or equivalent combination of education and experience • Demonstrated programming skills in SAS, including experience developing reproducible analysis pipelines • Demonstrated experience analyzing patient-reported outcome data in clinical trials, including application to the estimand framework • Background in biostatistics or related quantitative disciplines • Knowledge of Good Clinical Practice (GCP), quality assurance principles, and regulatory environments • Strong analytical, organizational, and problem-solving skills • High level of written and verbal communication skills • Ability to manage multiple tasks, meet timelines, and work effectively in collaborative team environments • Preferred: Experience in the pharmaceutical industry • Preferred: Experience interacting with regulatory agencies, including FDA, EMA, or other global health authorities • Preferred: Familiarity with R, machine learning, and natural language processing • Preferred: Experience with causal inference methods, including propensity score methods, weighting, marginal structural models, and external control arm studies

🏖️ Benefits

• Competitive base salary • Generous paid time off policy • Merit based annual increases • Bonus opportunities • Robust recognition program • Competitive insurance plans, including health, dental, life, and short-term and long-term disability • Retirement savings program such as a 401(k) plan • Paid parental leave for all parents • Financial assistance with adoption expenses or infertility treatments • Financial reimbursement for education and developmental opportunities • Employee assistance program • Other offerings to support a healthy work-life balance

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