Full-Time

Senior Statistical Programmer

Late Stage Development, Oncology

Posted on 3/13/2025

MSD

MSD

Compensation Overview

$111.4k - $175.3kAnnually

+ 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 on-site per week.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
SAS
Data Analysis
Requirements
  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field and at least 5 years SAS programming experience in a clinical trial environment
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field and at least 3 years SAS programming experience in a clinical trial environment
  • Effective interpersonal skills and ability to negotiate and collaborate effectively
  • Effective written, oral, and presentation skills
  • Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
  • A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders
  • Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise
  • Ability to comprehend analysis plans which may describe methodology to be programmed, an understanding of statistical terminology and concepts
  • Familiarity with clinical data management concepts
  • Experience in CDISC and ADaM standards
  • Experience ensuring process compliance and deliverable quality
  • Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices
  • Ability to anticipate stakeholder requirements.
Responsibilities
  • Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices
  • Maintain and manage a project plan including resource forecasting
  • Coordinate the activities of a global programming team that includes outsource provider staff
  • Membership on departmental strategic initiative teams
Desired Qualifications
  • Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life cycle (SDLC)
  • US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables
  • Experience assuring programming consistency across protocols and projects, directing the program development effort of other programmers; experience as a programming mentor
  • Ability and interest to work across cultures and geographies
  • Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
  • Experience developing and managing a project plan using Microsoft Project or similar package
  • Active in professional societies
  • Experience in process improvement

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A