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Senior Clinical Data Coordinator

2+ years
₹12,00,000 – ₹18,00,000 per annum
10 May 23, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Data Coordinator
Location: Hyderabad, India
Job Type: Permanent, Full-time
Estimated Salary: ₹12,00,000 – ₹18,00,000 per annum (based on industry benchmarks for similar roles in Hyderabad)

About the Role:

As a Senior Clinical Data Coordinator (CDC) at Sanofi, you will be responsible for ensuring high-quality clinical data throughout the study lifecycle, in line with GCP and applicable regulatory guidelines. You’ll work in close collaboration with Study Data Managers and cross-functional teams to ensure timely and accurate data delivery.

Major Responsibilities:

  • Perform data management activities including data validation, data review, and cleaning in accordance with study timelines.

  • Monitor progress of data cleaning and generate status reports for the Study Data Manager and clinical study team.

  • Contribute to the development of study documentation such as the Data Management Plan (DMP), Centralized Monitoring Plan, and UAT plans.

  • Execute and document User Acceptance Testing (UAT) for databases, listings, and safety tools, and provide feedback to the programming team.

  • Conduct centralized monitoring activities per the approved Centralized Monitoring Plan.

  • Communicate clearly on data management activities at the study level, including risk identification and escalation.

  • Act as a mentor to new Clinical Data Coordinators and identify opportunities to improve processes and data quality.

  • Provide support and serve as a back-up for the Study Data Manager when required.

  • Contribute ideas for new initiatives and improvements within the data management team.

Qualifications:

  • Education: Bachelor’s degree or higher in Life Sciences or a related discipline.

  • Experience: Prior experience in Clinical Data Management is essential.

  • Technical Skills:

    • Proficiency in clinical data systems and tools.

    • Knowledge of data management regulations and best practices.

    • Intermediate-level proficiency in Microsoft Office Suite.

  • Soft Skills:

    • Strong attention to detail and accuracy.

    • Effective communication (written and verbal).

    • Team-oriented with strong collaborative abilities.

  • Languages: Good command of English (verbal and written).

Why Choose Sanofi:

  • Join a forward-thinking, global biopharmaceutical company with strong growth prospects.

  • Contribute to cutting-edge innovations in Clinical Data Management.

  • Be part of a purpose-driven organization that values diversity, equity, and inclusion.

  • Unlock opportunities for personal and professional development.

  • Access a comprehensive rewards package and international career possibilities.


Sanofi is an equal opportunity employer. We value diversity and inclusion across all roles.