Associate Implementation Consultant

China, SH, Shanghai
Contratto a tempo indeterminato

Competenze principali del ruolo
Location:
China, SH, Shanghai
Job type:
Contratto a tempo indeterminato
Brand:
MEDIDATA
Experience level:
0 to 3 years
Posted on:
7/10/2025
Ref ID:
544610

About our Company:

Medidata: Powering Smarter Treatments and Healthier People

Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 36,000 trials and 11 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million users trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. Discover more at www.medidata.com.

About the Team:

 

Associate Implementation Consultants (AICs) will report to Manager of Implementation Consulting, will help ensure that Medidata’s software applications are implemented and configured following Medidata standard business processes, meet client requirements and applicable standards. IC’s also consult with our clients and provide guidance on how to best implement Medidata’s software to provide the most value.

 

AIC will be working alongside Project Managers and other functional departments during the implementation or enablement of Medidata’s software applications.

 

Responsibilities:

 

  • Support ICs in configuring or enabling customers on Medidata software to translate customer needs and meet customer requirements.
  • Adhere to or educate on best practices for implementing Medidata’s software.
  • Contribute to, 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 developers and other cross functional departments during configuration or implementation of specifications.
  • Support cross functional departments with issue resolution.
  • Shadow and work towards the delivery of in-person/remote client workshops.
  • Work to meet Project Management timelines and ensure timely completion of deliverables.
  • Support customers during enablement or implementation of our software by answering questions, resolving configuration or UAT issues, and providing guidance on software usage
  • Adhere to industry 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 internal initiatives, e.g., process improvement, product improvement, and identifying best practices.
  • Comply with and enforce Medidata Standard Operating Procedures, processes and policies.

Qualifications:

  • 4 -year college degree required (analytic discipline a plus)
  • 1-3 years relevant experience in clinical/biomedical or software development environment
  • Electronic Clinical Data Management (eCDM) software consulting experience desirable
  • Good experience working with clinical trials in a data management-related role, or equivalent combination of education and experience
  • Experience supporting project teams and meeting project timelines

 

Inclusion statement

As a game-changer in sustainable technology and innovation, Dassault Systèmes is striving to build more inclusive and diverse teams across the globe. We believe that our people are our number one asset and we want all employees to feel empowered to bring their whole selves to work every day. It is our goal that our people feel a sense of pride and a passion for belonging. As a company leading change, it’s our responsibility to foster opportunities for all people to participate in a harmonized Workforce of the Future.
MEDIDATA Logo > Dassault Systèmes

MEDIDATA genera le evidenze e le informazioni necessarie per aiutare le aziende farmaceutiche, biotecnologiche, di dispositivi medici e di diagnostica e i ricercatori nelle università ad accelerare il valore, ridurre al minimo i rischi e ottimizzare i risultati.

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