Job Description
A Life Science company based in San Diego, CA is seeking a Principal Technical Project Manager to join their team. Leads cross-functional teams to address business systems needs/issues. Plans and directs the analysis of complex business problems to be solved with automated systems. Provides technical leadership in identifying, recommending and evaluating systems and procedures that are cost-effective and meet user requirements. Plans and leads unit integration and acceptance testing; and may create specifications for systems to meet business requirements. Provides consultation to users in the area of automated systems.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Required Skills & Experience
• Bachelor’s Degree in computer science, IT or related field and 8+ years of relevant experience OR master’s degree in computer science, IT or related field and 6+ years of relevant experience
• Project Management Certification highly preferred
• 8+ years of Technical Project management experience (working in a pharmaceutical company with exposure to FDA regulations preferred)
• Experience managing technical implementation projects in support of business applications
• Experience with cloud-based softwares/platforms (Veeva, ServiceNow, NetSuite)
o Familiarity of Veeva and it’s support functions including: clinical, quality, safety& regulatory
• Experience with ERP
• Experience with Microsoft applications technologies such as MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, and
• Experience with Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming.
• Experience supporting validated systems/validation applications for regulatory purposes in a biotech/pharmaceutical company.
• Strong understanding of Technical projects with familiarity of web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.