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Sr. Scientist, Statistical Programming - Early Oncology; Hybrid

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: MSD Malaysia
Full Time position
Listed on 2025-12-22
Job specializations:
  • IT/Tech
    Data Analyst, Data Scientist, Data Science Manager
Job Description & How to Apply Below
Position: Sr. Scientist, Statistical Programming - Early Oncology (Hybrid)
** Responsibilities:
**** Education and Minimum Requirement:
*** BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS/R programming experience in a clinical trial environment
* MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS/R 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
* Designs and develops complex programming algorithms
* Ability to comprehend analysis plans which may describe the 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
* Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)
* Oncology clinical trial programming experience is preferred.
* AI/Machine learning experience and knowledge is preferred.
* 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
** Los Angeles Residents Only:
** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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