Global consulting firm has opportunities for Life Sciences Business Consultants (LBC) focused on Regulatory Submissions to help develop leading edge solutions to address enterprise wide requirements. This is a full-time permanent employment role requiring specific knowledge of the Regulatory Submissions process where you have been involved in the management of the life cycle of submission applications. You will have responsibility for contributing to the success of solution design/construction/implementation and integration. You will need to utilize your in-depth knowledge of leading-edge products and technology in conjunction with Regulatory Submissions and business skills to develop solutions in complex enterprise environments.
If work-life balance along with flexibility on where you can live is important, you can reside in any of the following major US cities: Atlanta, Boston, Charlotte, Chicago, Cincinnati, Columbus, Cleveland, Dallas, Denver, Detroit, Hartford, Houston, Kansas City, Los Angeles, Miami, Minneapolis, New York City, Philadelphia, San Francisco, Tulsa or Washington DC. You can live within a reasonable commuting distance (generally 50 miles) of one of these major airports. Weekday travel is typically three nights away from home with an emphasis on achieving a satisfying work-life balance. Occasional weeks may require four nights.
Experience: Here is a summary of what you must have before being considered. Please review carefully and submit your resume if you meet the following criteria
. 8 years experience in Life Sciences application development and lead developer responsibilities for at least 2 engagements in a consulting environment
. experience in the Life Sciences Industry with one or more of the following: Content Management (e.g. Documentum, OpenText LiveLink, CoreDossier, EZSubs, FileNet, etc.), Clinical Trial Management (e.g. Siebel eClinical, ClinPhone TrialWorks), Laboratory Information Management Systems (e.g. Labware LIMS, Applied BioSystemsSQL*LIMS) or Clinical Electronic Data Capture (Medidata RAVE, PhaseForward InForm)
. Technical qualifications include experience with application technical design and development, development of client solutions using a variety of development methodologies and tools (Java, J2EE, Visual C++, Java Script, Visual Basic), software package evaluation, management of client relationships and project plans, and strong verbal, written and communication skills
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