Full-Time

Sr. Scientist

Statistical Programming-Oncology

Confirmed live in the last 24 hours

MSD

MSD

Compensation Overview

$114.7k - $180.5kAnnually

+ Bonus + Long Term Incentive

Senior

H1B Sponsorship Available

North Wales, PA, USA + 1 more

More locations: Linden, NJ, USA

Hybrid work model requires three days in-office per week.

Category
Physicians & Surgeons
Medical, Clinical & Veterinary
Required Skills
SAS
Data Science
Data Analysis

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Degree
Experience
Requirements
  • Master’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or a related field and 3 years of experience in the position offered or related occupation
  • Bachelor’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Life Sciences, and 5 years of experience in the job offered or related occupation
  • 3 years of experience with SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH
  • 3 years of experience developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
  • 3 years of experience working with SAS systems and statistical databases
  • 3 years of experience designing and developing complex programming algorithms
  • 3 years of experience with analysis plans which describe the methodology to be programmed
  • 3 years of experience applying statistical terminology and clinical data management concepts
  • 3 years of experience with CDISC SDTM and ADaM standards
  • 3 years of experience ensuring process compliance and deliverable quality
  • 3 years of experience designing statistical databases with objective to optimize analysis and reporting and leverage departmental standards and industry best practices
  • 1 year of experience with oncology clinical programming support
Responsibilities
  • Utilize big data to analyze the safety and efficacy claims of potential medical breakthroughs
  • Support statistical programming activities for Early Oncology clinical development projects
  • Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials
  • Responsible for the development and execution of statistical analysis and reporting deliverables (e.g., safety and efficacy analysis datasets, tables, listings, figures) for early oncology studies
  • Responsible for design and maintenance of statistical datasets that support multiple stakeholder groups, including clinical development and safety evaluation
  • Collaborate with statistics and other project stakeholders in ensuring project plans are executed efficiently with timely and high-quality deliverables
  • Effective analysis and report programming development and validation, utilizing global and therapeutic area (TA) standards and following departmental standard operating procedures (SOPs) and good programming practice
  • Maintain and manage a project plan including resource forecasting
  • Coordinate the activities of a global programming team that includes outsourced provider staff

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