Source Job

• 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.

• Provide expert technical support and leadership in clinical trial reporting using advanced SAS features.
• Perform quality control checks and ensure accuracy and consistency of SAS code and output.
• Collaborate with cross-functional teams to support electronic submissions and compliance with regulatory standards.

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. With over 30 years of history, the company is consistently recognized as one of the industry's top places to work, including 14 consecutive years on Science magazine's Top Employers list and one of Fortune’s 100 Best Companies to Work For.

• Lead statistical activities for clinical trials, primarily in Oncology, and act as the lead statistician overseeing strategy and deliverables.
• Author key documents including Statistical Analysis Plans (SAPs), Analysis Database Specifications, and statistical sections of clinical study reports.
• Collaborate with cross-functional teams, communicate results to stakeholders, and ensure regulatory compliance with FDA, ICH, and GCP standards.

ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience and 4,000+ professionals across 20+ countries, we foster a quality-driven, one-team culture with below-average turnover and a focus on continuous training.

• Lead the full scope of Biostatistics activities for assigned clinical programs, including study design, analysis, and regulatory submissions.
• Collaborate cross-functionally with Clinical, Medical, and Regulatory teams to ensure quality and timely delivery of statistical outputs.
• Oversee CROs and internal teams, supervise statistical programming, and drive continuous improvement in biostatistics processes.

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote organization.

• 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.

• 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.

• 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.

• Develop and quality-control SDTM datasets supporting clinical research and regulatory submissions.
• Program complex SDTM datasets and trial design domains using SAS.
• Collaborate with sponsors, data operations, and cross-functional teams to ensure timely project delivery.

This partner company is a clinical research organization that develops SDTM datasets for regulatory submissions. The environment is collaborative, fast-paced, and focused on quality and operational excellence.

• Provide high-level consulting services for statistical analysis, reporting, and programming in clinical trials.
• Develop and validate statistical analysis plans, randomization schedules, and clinical trial reports.
• Mentor statistical programmers and ensure compliance with regulatory guidelines like ICH, GCP, and 21 CFR Part 11.

eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. It is a fast-growing company that has won the 2025 Top Workplaces USA Award for Remote Work and emphasizes an inclusive culture and work-life balance.

• 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.

• Design and review statistical methodology for clinical trial protocols and analysis plans.
• Lead execution of statistical analyses for regulatory submissions and exploratory studies.
• Effectively convey complex statistical concepts to cross-functional teams and stakeholders.

Natera is a global leader in cell-free DNA testing for oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply about their work and each other.

• 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.