Technical Consultant/ Clinical Data Analyst EMEA
il y a 3 jours
Yseop is recognized as the world-leading AI software company and pioneer in Generative AI. With a suite of industry-specific applications and cutting-edge hybrid Natural Language Generation (NLG) technology that blends symbolic, machine learning, and LLM techniques, Yseop ensures that even the most demanding content automation tasks are met with ease, scalability and application security across the entire enterprise.
At Yseop, our mission is to support companies through this digital transformation. As part of the organization, and our growing team, you will be in a unique position to impact the future direction the company takes and be a real asset to Yseop growth in Europe, continuously innovating and improving.
You’ll report to the Head of EMEA Customer Success based in Paris and join a global, diverse and international team of Consultants, Project Managers and Customer Success Managers based both in Paris and New York City.
YSEOP has developed a unique solution that provides automated drafted analysis based on Clinical Data, and therefore enables to dramatically accelerate the production of the regulatory documents required for Drug submission.
YSEOP is looking for a Clinical Data Analyst to support its Pharmaceutical customers during the implementation of YSEOP solution as well as supporting Clinical Studies production for submission.
YSEOP Clinical Data Analyst’s responsibilities include:
Coordination between our client’s Medical Writers, Biostats, and technical teams to coordinate and support the preparation and submission of clinical documents
Clinical data analysis, mapping and transformation into YSEOP’s data model and format
QC & Troubleshooting ensure delivery of automated draft documents ready-to-use by Medical Writers
Being solution-oriented and serving as a client advocate to YSEOP Product Management, Support, and Engineering to help drive toward successful and timely resolutions
Advocate best practices standards for Clinical Data Management
1 years experience in a Contract-Research-Organization or Pharmaceutical company as a Statistician programmer, Clinical Data Manager, Clinical Data Analyst or Business Analyst
~ Thorough knowledge of clinical data formats and modelization (SDTm, CDISC, AdAM)
~ Global vision of the clinical documents workflow that support Drug submission and pharmacovigilance processes
~ Excellent verbal and written communication skills (Fluent French & English required)
#Birthday Off and Mental Health Day
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