Full-Time

Associate Principal Scientist

Confirmed live in the last 24 hours

MSD

MSD

Compensation Overview

$135.5k - $213.4kAnnually

Senior

H1B Sponsorship Available

North Wales, PA, USA + 1 more

More locations: Linden, NJ, USA

Hybrid work model requiring three days in the office per week.

Category
Physicians & Surgeons
Medical, Clinical & Veterinary
Required Skills
Data Analysis
Requirements
  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 or more years of SAS programming experience in a clinical trial environment
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 or more years of SAS programming experience in a clinical trial environment
  • Excellent interpersonal skills and ability to negotiate and collaborate effectively
  • Excellent written, oral, and presentation skills
  • Broad knowledge and significant experience in developing analysis and reporting deliverables for Research & Development (R&D) projects (data, analyses, tables, listings, figures)
  • Strong project management skills; leadership at a program level; determines approach and ensures consistency and directs development of others when opportunities arise; ability to engage key stakeholders
  • Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH and familiarity with at least one other statistical computing software
  • Knowledge and understanding of CDISC SDTM and ADaM standards
  • Experience working with analytical research databases including various analysis datasets and procedures
  • Demonstrated understanding of statistics, clinical trial, and data management concepts as applied to drug/vaccine development
Responsibilities
  • Develop and validate global programming standards for ADaM datasets
  • Develop and validate global programming standards for efficacy analysis and reporting
  • Develop and validate global programming standards for safety analysis and reporting
  • Design and develop complex programming algorithms
  • Provide technical consultation and analytical support to statistical programmers and statisticians
  • Represent our Company on relevant industry initiatives including R Consortium, TransCelerate, PHUSE, CDISC
  • Collaborate with key stakeholders, partners in driving Analysis & Reporting standard programs using our Company standards, processes

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A