Lead data management activities for clinical and epidemiologic research studies from start-up through closeout.
Perform advanced SAS programming to clean, validate, and manage complex research datasets.
Design and maintain study databases, validation rules, and data quality procedures.
DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering, and digital transformation. The company employs experts in public health and health operations and is committed to innovation and improving lives.
Lead the development and execution of statistical analysis plans for large-scale real-world evidence studies.
Work directly with cross-functional teams and senior stakeholders to design data-driven solutions for a high-profile sponsor.
Oversee and mentor junior analysts, driving best practices and innovative analytics workflows.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, the company emphasizes a supportive culture, continuous training, and below-industry-average turnover rates.
Work with a national professional healthcare organization and educational/consulting organization to examine technology affordance and long-term cost-effectiveness.
Assist PI in development of survey design and qualitative protocol-specific tools for data collection and study documentation.
Conduct interviews and work with healthcare experts to obtain data, preprocess and analyze data using regression and optimization techniques.
Babson College is a world-class business school, empowering entrepreneurial leaders to create great economic and social value - everywhere. Here you’ll find a collaborative, collegial team environment designed to include and motivate every individual.
Provide statistical support for clinical trials, including protocol design, analysis plans, and database monitoring.
Serve as biostatistics lead for studies, publications, and regulatory submissions.
Ensure study designs are scientifically sound and meet regulatory requirements for efficacy and safety.
Replimune is a biotechnology company pioneering oncolytic immunotherapies to transform cancer treatment. Founded in 2015, the company values collaboration, boldness, dedication, and honesty.
Provide statistical support for HEOR, RWE, and Market Access activities under the guidance of senior leadership.
Collaborate with cross-functional teams to design studies, analyze data from clinical trials, claims databases, and registries.
Apply statistical methodologies and SAS/R programming to transform data into actionable insights for decision making.
Travere Therapeutics is a biopharmaceutical company dedicated to identifying, developing, and delivering life-changing therapies for people living with rare diseases. The company fosters a collaborative, diverse, and fast-paced culture with a global team that is passionate about making a difference for rare patients.
Develop and maintain clinical data listings, reports, and programming solutions to support data review and safety monitoring.
Analyze requirements from Data Management and Risk-Based Study Management teams and create efficient programming solutions.
Ensure all activities comply with regulatory requirements, industry guidelines, and internal procedures.
A partner company in the clinical research industry supports global clinical research programs through data analysis and programming. The company offers a fully remote, collaborative environment with a focus on continuous learning and improvement.
Lead statistical programming activities for Phase I–IV clinical studies across therapeutic areas.
Develop and maintain CDISC-compliant SDTM and ADaM specifications and SAS programs.
Mentor junior programmers and ensure regulatory compliance for submissions.
The partner company is a clinical research organization focused on driving healthcare innovation through clinical trials. The company's size and culture are not specified in the posting.
Leads a global team of Statistical Programmers, overseeing SDTM, ADaM, and TLF deliverables.
Ensures quality, budget, and timeline adherence while mentoring team members.
Contributes to process improvements and strategic initiatives to enhance operational efficiency.
Ergomed is a specialist clinical research organization focused on rare disease and oncology clinical trials. They have built a collaborative, international team across multiple continents, valuing teamwork, flexibility, and work-life balance.