Coordinating study data integration activities for the data flow implementation with external providers and internal stakeholders: specifications, implementation, testing including data collected through Central Labs, eCOA, IRT, connected devices, telemedicine, HR, and mobile healthcare.
Liaising directly with internal customers (Clinical Data Manager, Global Study Manager, Study Medical Manager, Statistician, Quality, etc.) and external providers to coordinate all clinical data integration activities for studies and discussing timelines.
Proactively anticipating and addressing data integration issues arising during study conduct and monitoring them until resolution.
Identifying areas for continuous improvement and actively participating.
Analyzing new requirements from customers and proposing technical solution strategies.
Providing support in the implementation of specific data flows and offering assistance to new Data Integration Analysts.
About you
At least 3 years’ experience in clinical data management and more than 1 years in external data integration and mapping.
Good collaboration and communication skill. Strong experience with CDM and related regulations (incl. ICH E6 and E8).
Solid risk-based mindset focusing on Quality by Design (QbD) and on what really matters.
Learn and adapt quickly when facing new problems. Think critically and use rigorous, objective, and pragmatic methods to solve multidimensional problems with effective and timely solutions.
Experienced in CDISC standards /terminologies in Clinical Data Standards. Good knowledge in data transfer and data mapping using digital tools.
Anticipate delivery risks, bottlenecks, issues, and delays to proactively prevent them or minimize their impact.
Understanding of advanced drug development concepts such as Decentralized Clinical Trials (DCT), Master & Adaptive Protocols, eSource. Programming languages (SAS, R or Python) and AI Based automations is a plus.
Bachelor or Master of Science degree or above, preferably in a life science or mathematics-related area (e.g., Pharmaceutical, medical, or mathematics, computer science or similar technical fields).
Strong English skills (verbal and written), ability to exchange fluently in a global environment.
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Join an international innovative biopharma company. Lead a clinical data technology team working on several therapeutic areas. Participate in the evolution of Clinical Data Management and deployment of innovations
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
