Sanofi Clinical Trial Coordinator Job Opening – Apply Online
Clinical Data Coordinator
Hyderabad, India
Permanent
Posted on: Feb. 04, 2025
Closing on: Feb. 14, 2025
Job title: Clinical Data Coordinator
Location: IN / Hyderabad
Grade: L1-1
About the job
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 Clinical Data Coordinator within our CDM Group…
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 Duties and 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 feedbacks 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).
About you
Experience: Experience on 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:
- 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).
Languages: Good English skills (both verbal and written).
Education: Bachelor’s degree or above, preferably in a life science or drug development related field.
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