About The Position

Are you ready to elevate your career by driving impactful change across dynamic cross-functional teams? As an IT Project Manager, you will dive into complex business challenges, crafting automated system solutions that propel our organization forward. You'll be at the forefront of innovation, providing expert analysis and technical guidance to optimize our systems and processes. From executing unit integration and acceptance testing to designing specifications that align with user needs, your expertise will be instrumental in our success. Be the catalyst for change and join us in delivering cutting edge solutions that are as cost-effective as they are transformative.

Requirements

  • BS/BA degree in computer science, IT, or similar Field and 2+ years of IT experience; working in a pharmaceutical company with exposure to FDA regulations preferred.
  • Recent experience implementing and in support of business applications, including Microsoft applications, preferred utilizing some or all the following technologies: MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, and Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming.
  • Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company preferred.
  • Some experience with web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data warehousing/data mining a plus.
  • OR Master’s degree in computer science or IT preferred and some related experience noted above.
  • PMP certification or working towards.
  • Comfortable with tools and processes that support work conducted by functional area.
  • Strong computer skills.
  • Ability to meet deadlines.
  • Good project management skills.
  • Ability to motivate a cross-functional business and technical project team.
  • Excellent verbal, written, and interpersonal communication skills, including the ability to work collaboratively with all employee levels as well as external contacts (vendors).
  • Excellent decision-making, conflict-resolution and influencing skills.
  • Good knowledge of Microsoft applications / data base and programming technologies.
  • Good knowledge of with web technologies such as HTML, XML, or latest mark up language Visual Basic / Java based or similar language and Internet Database Programming.
  • Knowledge of validated applications for regulatory purposes in a biotech/pharmaceutical company.
  • Familiarity with web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data warehousing/data mining.
  • Understands Neurocrine's business objectives and developing understanding of Neurocrine's services and customers.
  • Has experience in specific functional discipline while working to acquire higher-level knowledge and skills.

Responsibilities

  • Participates on project teams in the capacity of supporting application implementation, administration, and support.
  • Reviews and assists in the development of processes required for the successful implementation of key software systems.
  • Provides support for the management of data from multiple sources and databases for the eventual submission to multiple regulatory agencies.
  • Interacts with Clinical and Regulatory departments on issues relating to electronic submissions.
  • Supports evaluation and implementation of additional technologies that may improve the overall quality of systems throughout all departments.
  • Consults with department representatives to determine requirements for data access, reports, and interfaces.
  • May interact with department managers, typically works with main system users to assess implementation of data management/interface tools.
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