Participate in CRF design, database review, and data validation procedures to ensure data integrity.
Produce data listings, summary tables, and graphics for interim and final analyses of clinical trials.
Collaborate with Biometrics functions and coordinate data transfer standards with CROs and vendors.
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 across the Americas, Europe, and Asia-Pacific, they maintain a supportive culture focused on quality, professional development, and low turnover.
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.
Conduct real-world studies including data feasibility assessments, protocol development, analyses, and study reports.
Perform data preparation and analyses independently and make recommendations to clients and team members.
Contribute to multiple cross-functional projects and communicate study results internally and externally.
Precision AQ is a healthcare research company specializing in real-world evidence studies for the pharmaceutical and biotech industry. Their dynamic team of research professionals focuses on improving healthcare outcomes worldwide.
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.
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.
Lead analytical projects from requirements gathering through implementation, partnering with service centers and product owners to improve customer and employee experiences.
Analyze KPIs, product releases, and service initiatives using quantitative methods such as A/B testing, and develop reports, dashboards, and analytical tools.
Mentor junior analysts and contribute to a collaborative team environment while presenting findings to stakeholders and senior leadership.
Liberty Mutual is a global insurance provider offering personal and commercial insurance products. With thousands of employees, the company fosters an inclusive culture where employees can thrive and make an impact.
Provide statistical oversight and lead complex programs such as NDA/BLA/MAA submissions.
Consult with clients on clinical trial study design and regulatory strategy.
Author statistical analysis plans and review statistical output for accuracy.
Precision Medicine Group provides statistical leadership and support for clinical development, consulting with clients on trial design and regulatory strategy. The company is a global organization that values collaboration, service, and accountability, fostering a culture of mentoring and innovation.
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.
Design, develop, and validate CDISC-compliant SDTM and ADaM datasets for clinical trials.
Support regulatory submissions including ISS, ISE, and create Tables, Listings, and Figures.
Collaborate with cross-functional teams to deliver accurate statistical outputs for evidence-based healthcare.
The partner company is a clinical research organization that supports impactful clinical programs through statistical programming. It offers a collaborative culture and a flexible remote work environment.
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.
Serve as the site manager, ensuring data entry and query resolution, and maintain high-quality data and audit readiness at clinical sites.
Monitor ongoing compliance to study protocols and site adherence to global regulatory guidelines, including safety reporting, both onsite and remotely.
Manage device accountability, inventory, distribution, and regulatory documentation to ensure compliance and audit readiness.
Penumbra is a global healthcare company focused on innovative therapies, designing, developing, manufacturing, and marketing novel products for challenging medical conditions. The company sells its products to hospitals and healthcare providers worldwide through direct sales and distributors.
Collaborate across sophisticated evidence synthesis projects, developing deliverables like protocols and technical reports.
Manage day-to-day client communications and delegate tasks to junior researchers.
Provide mentorship and direction while independently completing complex job responsibilities.
Precision Medicine Group is a global portfolio organization that provides evidence synthesis services for health technology assessments. The company has a start-up culture in a well-funded established organization.
Manage all programming aspects of clinical databases from study start to post-lock, ensuring compliance with regulatory guidelines.
Lead operational study teams and provide technical training to end users and junior staff.
Communicate project status to internal teams and clients, and perform project forecasting and budget management.
Precision for Medicine is a life sciences company that provides clinical research services, including database programming and data management. The company is growing and seeks a Principal Database Programmer to join its European team, fostering a collaborative and dynamic work environment.
Plan, lead, and oversee projects using project management processes to meet deadlines and budgeted costs.
Analyze and research business problems, design innovative solutions, and develop/maintain programs for the clinical data repository.
Collaborate with customers and IT, conduct tests, and provide off-hours support to ensure quality and service.
Capital Blue Cross is a health insurance company and independent licensee of the Blue Cross Blue Shield Association. They provide health insurance plans and services to members in Pennsylvania and are an equal opportunity employer.
Independently perform statistical analyses for clinical studies and research initiatives.
Develop statistical analysis plans, including sample size and power calculations.
Collaborate with cross-functional teams to ensure statistical rigor and appropriate interpretation of results.
Karius is a life science, venture-backed clinical metagenomics company focused on elevating patient care through microbial insights. The company delivers unprecedented diagnostic insight detecting microbial cell-free DNA to assist physicians in making rapid treatment decisions.
Analyze complex healthcare data sets including Medicaid eligibility, claims, and enrollment to drive policy decisions.
Develop dashboards, monitoring tools, and reports for state government healthcare agencies.
Collaborate with multidisciplinary teams to translate analytic findings into actionable insights for decision-makers.
BerryDunn is a client-centered, people-first professional services firm that helps businesses, nonprofits, and government agencies solve challenges. The firm has been recognized for its diverse and inclusive workplace culture and focus on learning, development, and well-being.