We are hiring a Data Analyst to maintain databases and master data for one of our pharmaceutical client's product research wing. The data analyst will utilize established processes and serve as a key technical resource at the operational level. They will drive master data solutions for the local site. They will also provide on-going support for completing tasks associated with the SAP master data/specification responsibilities and projects including but not limited to the following:

  • Execute data collection, data entry, data verification, and data cleansing in SAP and associated systems per established processes and procedures
  • Second person verify SAP master data entries for new master data requests and changes to existing data.
  • Assist in creation and maintenance of material specifications managed by the product research group.
  • Use change management process and tools.
  • Create, change, maintain, and inactivate SAP master data utilizing established processes, tools, and procedures.
  • Assist with Periodic Review of material specifications and update appropriate systems per established processes and procedures.
  • Be proactive in maintaining data accuracy in recognition of its criticality to running our business.
  • Identify and address issues as they arise, and escalate them to supervision and/or business sponsor when issues are outside of one's scope to remedy.
  • Be able to train others on tasks they perform.
  • Comply with local and global SOPs/policies.
  • Maintain a safe work environment, working safely and accountable for supporting all Health Safety and Environmental Corporate and Site Goals.
  • Maintain learning plan at a 100% compliance level in accordance with all government regulations and Global Policies and Procedures


  • Experience with SAP master data entry
  • Strong attention to detail and work accuracy
  • Strong organizational skills
  • Ability to manage multiple priorities and meet timelines
  • Ability to build collaborative working relationships
  • Knowledge of and compliance with GMP requirements
  • Critical thinking and problem solving skills
  • Good written and verbal communication skills
  • Learning agility and self-management skills
  • Ability to learn a variety of IT systems and tools (e.g. SAP, cMat, Excel tools, Trackwise, SharePoint, Regulus) General business understanding of clinical trial data governance and supply chain
  • Quality background is helpful.


  • 16 days of PTO
  • Medical, Dental and Vision benefits
  • 401(k) enrollment option with 3% employer matching
  • Apply Now
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