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Job Details

Skills

Collaboration
Biostatistics
Data Cleansing
SAS/MACROS
SOP
Training
Documentation
Leadership
Data Engineering
SAS
Business Objects
Crystal Reports
CDISC
Google Cloud Platform
Google Cloud
SFTP
FTP

Summary

Responsibilities:

Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications.
Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines.
Perform peer review of DRLs and data reconciliation reports.
Monitor automated job logs and resolve issues as needed.
Retrieve and post external vendor data using sFTP/FTP clients and vendor portals.
Collaborate with data managers, statistical programmers, biostatistics, and clinical operations to support data cleaning and integrity activities.
Contribute to the development and maintenance of SAS macro programs and departmental programming standards.
Participate in SOP and work instruction development, including program validation and documentation.
Provide guidance and support to junior members of the data programming team.

Requirements:

Bachelor's or Master's degree in a relevant field or equivalent experience.
7+ years of clinical data programming experience, with a minimum of 5 years in oncology.
Hands-on experience across Phase I, II, and III oncology trials.
Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports.
Familiarity with CDISC, 21 CFR Part 11, ICH, and Google Cloud Platform guidelines.
Experience with sFTP/FTP tools and vendor data portals.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: b53eee0a670d7ab22804769f0965f049
Posted 30+ days ago

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