Implementation Consultant, Patient Cloud

    • London, United Kingdom

Medidata: Conquering Diseases Together

 

Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 1,400 customers and partners access the world's most-used platform for clinical development, commercial, and real-world data. Medidata, a Dassault Systèmes company, is headquartered in New York City and has offices around the world to meet the needs of its customers. Discover more at www.medidata.com.

Your Mission: 

Implementation Consultants help ensure that Medidata’s software applications are implemented and configured in accordance with Medidata standard business processes, meet client requirements and adhere to Good Clinical Data Management Practices. ICs also consult with our clients, provide guidance and make suggestions on how to best implement Medidata’s software to provide the most value. 

The Implementation Consultants work with Project Managers and other functional departments during the implementation and configuration of Medidata’s software applications, in addition to helping in the training, education and mentoring of colleagues.

  • Configure Medidata software products to translate customer needs and meet customer requirements
  • Adhere to best practices for implementing Medidata’s software
  • Author, adapt, or agree on specifications based upon client requirements.  This can include functional test cases for use in configuring and developing solutions in Medidata’s suite of products, as well as in custom integrations
  • Support Associate Implementation Consultants (AICs) in the authoring of specifications, being accountable for quality of delivery 
  • Support developers and other cross functional departments during configuration or implementation of specifications
  • Delivery of in-person/remote client workshops
  • Work to Project Management timelines and budgets, ensuring timely completion of deliverables within the agreed scope of work
  • Support customers during the user acceptance testing cycle by resolving issues, and answering questions
  • Adhere to data collection and handling standards to ensure consistency and facilitate downstream processing (e.g., QC testing)
  • Communicate status reports to stakeholders on both client and internal projects
  • Participate in and lead internal initiatives, e.g., process improvement, product improvement, and identifying best practices
  • Comply with and enforce Medidata Standard Operating Procedures, processes and policies
  • Assist in the scheduling of professional services resources and ensure timely completion of deliverables
  • Support Training Group in preparation of course materials and delivery of courses both internally and externally as needed
  • Support third party vendors in defining Data Transfer Specifications
  • Own multiple customer facing projects
  • Work towards becoming a Subject Matter Expertise (SME) in at least one product/solution
  • Mentor/Train AICs or new employees


Your Competencies: 

  • Knowledge of Clinical Trial processes, specifically as they related to data collection, standards, management, and preparation for statistical analysis
  • Strong understanding of data management plans/customer specifications for data entry screens, edit checks, custom reports and data integrations
  • Ability to work with technical R&D staff and translate new software features into real world examples
  • Knowledge of computer usage in a web-based environment
  • Ability to think logically to solve complex problems 
  • Solid analytical and technical skills with regard to software applications
  • Strong collaboration and team-building skills
  • Excellent verbal and written communication skills
  • Strong organizational and time management skills
  • Self-motivated, able to assume responsibility and work autonomously in a professional manner
  • Experience of working to Standard Operating Procedures 
  • Adaptable to changing business needs and/or product landscapes


Your Education & Experience:

  • University/college degree or equivalent (analytic discipline a plus)
  • Experience working with clinical trials in a data management-related role, or equivalent combination of education and experience
  • Prior services delivery experience required
  • Experience supporting project teams and meeting project timelines
  • Electronic Clinical Data Management (eCDM) software consulting experience desirable
     

MDSOL Europe Ltd is an equal opportunity employer.  We welcome all applications irrespective of race, gender, gender reassignment, age, religion or belief, relationship status, pregnancy/maternity, sexual orientation or disability.



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Medidata powers the development of new therapies for more than 1,000 life science companies worldwide.

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