Job description

•       At Least 8+ years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business, or IT representative
•       In-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing and/or Viewing systems
•       Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction
•       Influential; experience leading teams through hard decisions and negotiating compromises
•       Technical abilities and willingness to “roll up your sleeves” to design and implement a RIM solution
•       Expert on life sciences compliance and computer systems validation requirements
•       Ability to work independently in a dynamic environment
•       Typical travel is 25% but may be up to 50% based on customer requirements

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