Job Title: Senior Clinical Data Coordinator (CDC)
About the Role
The Senior Clinical Data Coordinator (CDC) is responsible for performing routine data management activities throughout the course of a clinical study, ensuring compliance with GCP and applicable regulatory guidelines. The role ensures generation of accurate, complete, and consistent clinical databases.
As part of Sanofi’s global hubs, you will support innovation and performance improvement across departments, contributing to transforming lives worldwide. In this role, you will support the Study Data Manager in study data management activities, ensuring timelines are met and deliverables are of the highest quality.
Key Responsibilities
Ensure data quality by conducting data validation, data review, and other data management activities per study timelines.
Monitor progress of data cleaning activities and generate status reports for the Study Data Manager and study team.
Participate in the development of study-related plans (Data Management Plan, Centralized Monitoring Plan, etc.) within agreed timelines.
Contribute to User Acceptance Testing (UAT) plans; perform testing of databases, listings, patient profiles, and safety notification tools; provide feedback to programming team and Study Data Manager.
Conduct centralized monitoring activities as per the Centralized Monitoring Plan.
Ensure effective communication at study level, including risk identification, monitoring, alerts, and escalation.
Mentor new Clinical Data Coordinators (CDC) and identify process improvement opportunities to streamline workflows and enhance data quality.
Provide input on new approaches and initiatives within data management with a collaborative and motivated team spirit.
Act as a back-up to the Study Data Manager when required.
About You
Experience
Strong background in Clinical Data Management.
Soft Skills
High level of accuracy and attention to detail.
Excellent written and verbal communication skills.
Strong teamwork and collaboration abilities.
Technical Skills
Solid knowledge of Clinical Data Management (CDM) processes and regulatory guidelines related to data quality and clinical trial conduct.
Familiarity with database technologies and eagerness to acquire new technical skills.
Proficiency in Microsoft Office Suite (intermediate level).
Education
Bachelor’s degree or higher, preferably in life sciences, drug development, or a related field.
Languages
Proficiency in English (written and spoken).
Why Join Us?
Be part of a supportive, future-focused team bringing the miracles of science to life.
Access limitless career growth opportunities—both locally and globally.
Receive a comprehensive rewards package that values your contribution.
Join an innovative, international biopharma company at the forefront of Clinical Data Management modernization.
Contribute to pioneering advancements in clinical research and data innovation.
About Sanofi
At Sanofi, our purpose is to chase the miracles of science to improve people’s lives. We are committed to equal opportunities and embrace diversity, equity, and inclusion.
“Our ambitions are significant but pragmatic. The speed of change is unprecedented but achievable. Join us if you want to help transform our vision into reality.”
Pursue Progress. Discover Extraordinary.
Join us and shape the future of science—while growing your career beyond what you thought possible.
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