**_About the job_** The Senior Clinical Data Coordinator (CDC) is responsible for routine data management activities during the course of a study complying with GCP and applicable regulatory guidance to ensure the generation of accurate, complete and consistent clinical databases. Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As **Senior Clinical Data Coordinator** within our Clinical Data Management, you’ll support the Study Data Manager in conducting study data management activities, ensuring his/her activities are completed per agreed timelines. Candidate is responsible for the quality of its own deliverables. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? **Major Responsibilities** **:** + Ensure data quality by conducting data management activities including data validation, data review, etc. following study timelines. Maintain clear reporting on DM activities in alignment with study teams and management needs. + Monitor the progress of data cleaning activities and generate status reports for the Study Data Manager and study team. + Participate in the writing of study plans including Data Management Plan, Centralized Monitoring Plan etc. as per timelines defined with the study team. + Participate in the writing of UAT Plans and perform testing for database, listings, patient profile and safety notification tool, providing feedback to programming team and Study Data Manager to collaboratively solve issues found both during initial database set up and database revision. + Conduct centralized monitoring activities according to Centralized Monitoring Plan. Ensure clear, concise, consistent communication on data management activities at study level (including risks identification, monitoring, alert and escalation) + Acts as mentor for new CDC. Identifies opportunities to streamline processes and increase data quality. + Provides input to new approaches and initiatives within data management activities, with a high level of team spirit and motivation. Support and act as back-up of the Study Data Manager, when requested. **_About you_** + **Experience:** Experience in Clinical Data Management. + **Soft skills:** Excellent accuracy and attentiveness to detail + Excellent written and oral communication + Good team player and ability to foster a good collaboration within CDM and with clinical study team + **Technical skills:** Strong experience with CDM and Knowledge of regulatory guidelines in relation to data quality and clinical trials conduct. + Knowledge of database technologies and ability to acquire and apply new technical skills. + Proficiency in Microsoft Office Suite (intermediate level) + **Education:** Bachelor’s degree or above, preferably in a life science or drug development related field. + **Languages:** Good English skills (both verbal and written). **_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. + Join an international innovative biopharma company. + Participate in the evolution of Clinical Data Management and deployment of innovations. **“Sanofi is at the forefront of the Clinical Data Management Modernization. Our ambitions are significant but pragmatic. The speed of change unprecedented but achievable. Join us of you want to help us transform our vision into a reality!”** **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 (https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at sanofi.com (https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness) ! Global Terms & Conditions and Data Privacy Statement (https://www.sanofi.com/en/careers/global-terms-and-conditions/) Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi (https://youtu.be/96EwNjb1TLo) As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live. All in for Diversity, Equity and Inclusion at Sanofi - YouTube (http://www.youtube.com/watch?v=SkpDBZ-CJKw&t=2s)