CSV Consultant

Job Title: CSV Consultant

Address the work will be performed: Redwood City CA 94065

Target start date: 4^th May.

Length of contract assignment: Until end of year 2026

Client Mid-size pharmaceutical Org

Location Redwood City CA 4 days onsite is required

Duration through EOY possible extensions

Work schedule/typical work week/daily start and end time:

• 8 am to 4 pm PT flexible
• On-site 4 days per week to start
  • Potential to flex to 3 after getting acclimated with team

Client description:

• This is a fast-growing pharmaceutical company with one approved product on the market currently.
• The client has two additional drug launches in 2026 and has almost doubled in company head count in less than 2 years.

Project description:

• Our client is in need of an experienced and well-rounded CSV Consultant to join their team and support 2 ongoing projects as well as additional projects across multiple systems.
  • SAS Studio Project Our client began a lengthy project of installing SAS Studio requiring them to internally manage AWS servers and migrate over. The consultant will own the validation portion of this project and need an understanding of how SAS Studio works and interacts with GxP data.
  • Data Migration Project The client is migrating data from their source system to their target system and creating a data migration plan/protocol. This will involve a lot of data clean up data conversion and field mapping. The consultant will need to utilize their knowledge of data migration tools theyve used in the past to develop a plan/approach for the migration and also be responsible for getting appropriate documentation in place.
  • Additional Projects: ETMF Update CTMS Updates Veeva QMS/QDS Projects Trace Link Project & Argus Projects.
• All of the above systems are validated except for SAS Studio. SAS Studio is currently going through the revalidation process. The main role of this consultant will be owning the validation for these projects.
• Team Breakdown: AD IT CSV 2 CSV Consultants and the Quality Team.

Technology environment the consultant will be working in:

• SAS
• CTMS Medidata
• Veeva Quality Docs
• TraceLink
• SharePoint
• Microsoft Office Excel Word Power Point Outlook

Required Skills:

• Previous experience as a CSV consultant at a pharmaceutical company to include:
  • Validating the Veeva Platform such as: QMS RIM or Quality Docs
  • Developing UATs and writing test scripts

• • Working with Veeva Change Control and understanding how the systems works with the ability to create change controls and close them
  • Working with SAS Studio and understanding how it works and interacts with GXP data
  • Working on data migration projects - knowledge of data migration tools developing a plan/approach for a data migration and getting appropriate documentation in place

Interview process:

• 2-3 rounds of 30-minute Teams Meetings