SENIOR STATISTICAL PROGRAMMER

Hired by Matrix, Inc.; Nutley (NJ); Hybrid; USD 100,000 - 130,000; Full time

Job summary

A global pharmaceutical company is seeking a Senior Statistical Programmer to join their team in Nutley, NJ. The ideal candidate will have extensive experience in programming and application development within the pharmaceutical sector. Responsibilities include annotating CRFs, ensuring quality assurance, and managing SDTM data production processes. This role offers the flexibility of remote work with occasional office visits. If you have a strong background in SAS and CDISC, this could be a great opportunity for you.

Qualifications

• Minimum 12 years of relevant programming experience in CRO, Pharmaceutical or Biotech.
• Expert in addressing technical challenges with SAS, CDISC and XML.

Responsibilities

• Annotate CRFs according to CDISC guidelines.
• Review and assure quality of CRF annotations and programming specifications.
• Accountable for SDTM data production processes.

Skills

SAS

CDISC

XML

Technical Skills

Education

Master's Degree in Computer Science

Master's Degree in Mathematics

Job description

Are you ready to build your career by joining a global pharmaceutical company. If so, our client is hiring a Senior Statistical Programmer.

Position Type : Contract

Remote : (Preference from northeast or in the same time zone and come to the Nutley office when there's a need)

Required :

• Minimum 12 years of relevant programming and application development experience in CRO, Pharmaceutical or Biotech organizations.
• Master's Degree in Computer Science or Mathematics or any relevant field.
• Expert in addressing technical challenges that connect SAS, CDISC and XML.
• Excellent technical skills in SAS system and application development.
• Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.
• Expert in integrating SAS with other leading technologies such as PDF, XML, Microsoft Office, to support electronic submissions.
• Experience in consulting projects dealing with the assessment, design and / or implementation of CDISC data standards in the clinical data life cycle.

Responsibilities :

• Annotate CRFs in accordance with CDISC published or company specific guidelines with appropriate metadata to reflect case report tabulation data sets.
• Review and quality assure CRF annotations produced by other programmers
• Embrace and contribute to our culture of process improvements with a focus on streamlining our processes adding value to our business needs.
• Review and quality assure data set and programming specifications produced by other programmers.
• Accountable for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission.
• Accountable for execution of process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission
• Engages appropriate stakeholders in communication to create SDTM standards and process for transition of clinical data to SDTM
• Accountable for SDTM datasets specification, conversion, and delivery to stakeholders, specifically Statistical Programming, but also other users of SDTM datasets, with high quality and on time.
• Provides SDTM data production technology to CDO (Clinical Data Operations) related to SDTM data delivery and manages the activities of a team with a common focus

Get in Touch :

If you think you'd be a good match, submit your resume and reach out to Priyanshu at [phone] to learn more.

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Senior Programmer • Nutley, NJ, United States