Source Job

US

  • Lead technical sales engagements with healthcare and life sciences clients, gathering requirements and demonstrating SLC capabilities.
  • Conduct proof-of-concept activities and provide architectural guidance for deploying SLC in existing IT ecosystems.
  • Act as a subject matter expert in SAS language and statistical programming, authoring industry-specific presentations and workshops.

SAS Statistical Programming Communication Python

10 jobs similar to Principal Global SLC Pre-Sales Consultant – Healthcare and Life Sciences

Jobs ranked by similarity.

$136,960–$205,440/yr
US

  • 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.

UK

  • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
  • Create datasets, tables, listings, and figures according to study requirements and CDISC standards.
  • Collaborate with Biostatistics, Data Management, and Clinical teams to ensure quality and timelines.

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 28 years of experience and 4,000+ professionals across more than 20 countries, we foster a supportive culture with below-industry-average turnover.

$158,000–$227,000/yr
US 3w PTO

  • Manage a team of statistical programmers supporting clinical research and ensuring quality, integrity, and timely delivery of programming deliverables.
  • Provide statistical programming support, oversee development of code for Tables, Listings, and Figures, and ensure compliance with quality processes.
  • Lead resource planning, manage CROs, and contribute to process improvements and innovation in statistical programming standards.

Penumbra is a global healthcare company focused on innovative therapies, designing and marketing novel products for challenging medical conditions. It sells primarily through a direct sales organization in the US, Europe, Canada, and Australia.

US

  • Serve as an embedded consultant and forward-deployed engineer at a pharmaceutical customer site to co-create analytics and AI-driven solutions on SAS technology.
  • Lead time-boxed innovation sprints to design and deliver production-ready capabilities, translating business challenges into scalable solutions.
  • Apply deep life sciences expertise to solve problems across R&D, clinical, manufacturing, and commercial operations.

SAS is a leader in data and AI, inspiring customers to transform data into intelligence through software and services. The company is recognized for its inclusive culture and innovative technologies, with a world-class employee experience.

US

  • 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.

US

  • 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.

$110,000–$140,000/yr
United States

  • 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.

US

  • 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.

UK

  • Lead and support statistical programming deliverables for oncology clinical studies.
  • Ensure high-quality programming with CDISC standards and regulatory compliance.
  • Collaborate with cross-functional teams including statisticians, data managers, and study leaders.

ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of experience and over 4,000 professionals in more than 20 countries, with a culture focused on quality, professional development, and supportive collaboration.

UK

  • Lead protocol development including study design and statistical analysis plans for clinical trials.
  • Provide statistical oversight, mentoring, and training to ensure high-quality project delivery.
  • Manage statistical activities across projects, ensuring accuracy and consistency with regulatory standards.

ClinChoice is a global full-service CRO specializing in clinical development for pharma, biotech, and medical device companies. With over 4,000 professionals across 20+ countries, they foster a quality-driven, one-team culture and emphasize diversity and low turnover.