Location: West Point, PA Area (Remote) (w2)
EXP - 3+years | Any Visa
Job Summary
OVERALL RESPONSIBILITIES:
Development and generation ofSASanalysis datasets, tables, listings, and graphs from assigned clinical sources; leading development and maintenance of associated operating procedures; and participating in external industry forums (e.g., CDISC, SCDM, and User Groups). This individual performs with minimal on moderately difficult deliverables.
POSITION DUTIES & RESPONSIBILITIES:
- Utilize programming standards to develop efficient and accurate programs.
- Support the maintenance of establishedSASplatform.
- Support the maintenance a globalSASmacro library.
- Work with Data Management leadership to provide input on reporting processes and standards.
- Support programming deliverables for clinical trials and support for any custom Data Management reports.
- Participate in the development and maintenance of global harmonized processes and procedures for programming.
- Work with BSDM partners, and leadership in Clinical Operations and Franchise to set implement plans for timely delivery of reports, metrics and study deliverables.
- Facilitate the delivery of standard metric reports.
- Ability to design, implement and maintain moderately complex programming deliverables across a wide variety of clinical platforms and therapeutic areas.
Functional and Technical Competencies:
- Proficiency in BaseSAS,SAS/STAT andSASMacro language. AdvancedSAScertification desirable. Experienceprogramming with R desirable.
- Demonstrated ability to work in teams to deliver critical milestones.
- Experience with CDISC datasets, tables, listings and figures desirable.
- Excellent verbal and written communication skills
- Connect – Participate in strategic partnerships with Clinical System and Biostatistics at the Enterprise level to ensure MD programming practices meet the needs of the organization.
- Shape – Develop knowledge of therapeutic areas within the Franchises and adapt ADaM and STDM standards for medical devices for use in the MD sector; participate in industry initiatives to define/refine STDM standards.
- Lead – Present opportunities in programming practices that increase quality of deliverables.
- Deliver – ensure high quality programming deliverables for clinical programs are delivered on time and in compliance to regulations and SOPs, seamlessly across all Franchises.
EDUCATION & EXPERIENCE REQUIREMENTS:
- A bachelor’s degree in Statistics, Computer Science or related discipline (required), with at least 5-6 years of system support in clinical research within Medical Device or Pharmaceuticals
Seniority level
Seniority level
Mid-Senior level
Employment type
Job function
Job function
Research, Analyst, and Information TechnologyIndustries
Software Development
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