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Senior Clinical Data Coordinator Vax

Sanofi · Hyderabad
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1d ago
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Job Title : Senior Clinical Data Coordinator

  • Location:Hyderabad

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. Join our Hyderabad Hub, build a career and you can be part of transforming our business while helping to change millions of lives. Ready? 

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.  

He/She supports the Study Data Manager in conducting study data management activities, ensuring his/her activities are completed per agreed timelines. 

He/She 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? 

 

Main responsibilities include: 

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) 

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  

  • Minimum of 4 years’ experience on clinical data management 

  • 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 

  • 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) 

  • 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. 

  • 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. 

  • Participate in the evolution of Clinical Data Management and deployment of innovations. 

 

Pursue Progress. Discover Extraordinary.   

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together. 

 

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.  
 

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! 

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!

Apply at Sanofi →