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Trainee Medidata Rave Programmer Jobs in California

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Trainee Medidata Rave Programmer information

What is the difference between Trainee Medidata Rave Programmer vs Junior Clinical Data Coordinator?

AspectTrainee Medidata Rave ProgrammerJunior Clinical Data Coordinator
Required CredentialsBasic knowledge of Medidata Rave, relevant coursework or certificationsDegree in life sciences or related field, some data management training
Work EnvironmentClinical trial data management teams, often in CROs or pharma companiesClinical trial sites or data management departments within pharma
Industry UsagePrimarily in clinical data management and EDC system setupData collection, validation, and quality control in clinical trials

The Trainee Medidata Rave Programmer focuses on learning and supporting EDC system setup and data entry using Medidata Rave, while the Junior Clinical Data Coordinator handles data validation and management at clinical sites. Both roles require familiarity with clinical data processes but differ in responsibilities and focus areas.

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Trainee Medidata Rave Programmer jobs near you
Infographic showing various Trainee Medidata Rave Programmer job openings in California as of August 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.

SAS Programmer

Katalyst Healthcares and Lifesciences

San Francisco, CA • On-site

Other

Posted 4 days ago

Job description

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.

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