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Senior Clinical Data Coordinator

2+ years
Not Disclosed
10 Oct. 16, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Senior Clinical Data Coordinator
Location: Hyderabad, India

About the Job
The Senior Clinical Data Coordinator (CDC) plays a vital role in ensuring the quality and integrity of clinical data throughout the study lifecycle. This position involves routine data management activities in compliance with GCP and applicable regulatory guidelines, contributing to the generation of accurate, complete, and consistent clinical databases.

As part of our innovative global healthcare team, you’ll help drive transformation while positively impacting millions of lives. Are you ready to take the next step in your career?

Major Responsibilities:

  • Ensure data quality through rigorous data management activities, including validation and review, aligned with study timelines.
  • Monitor data cleaning activities and generate status reports for the Study Data Manager and study team.
  • Assist in writing study plans such as Data Management Plans and Centralized Monitoring Plans.
  • Contribute to User Acceptance Testing (UAT) Plans and perform testing for databases, listings, patient profiles, and safety notification tools, providing feedback to the programming team.
  • Conduct centralized monitoring activities per the Centralized Monitoring Plan.
  • Communicate effectively about data management activities, including risk identification and escalation.
  • Mentor new Clinical Data Coordinators, identifying opportunities to enhance processes and data quality.
  • Support the Study Data Manager as needed and contribute to new initiatives within data management.

About You

  • Experience: Background in Clinical Data Management.
  • Soft Skills: Strong attention to detail, excellent communication skills, and a collaborative mindset.
  • Technical Skills: Proficient in clinical data management and regulatory guidelines; familiarity with database technologies and Microsoft Office Suite.
  • Education: Bachelor’s degree or higher in a life sciences or related field.
  • Languages: Proficient in English (both verbal and written).

Why Choose Us?

  • Join a supportive, forward-thinking team that brings the miracles of science to life.
  • Explore endless opportunities for career growth and advancement, both locally and internationally.
  • Enjoy a comprehensive rewards package that recognizes your contributions and enhances your impact.
  • Be part of an innovative biopharma company at the forefront of Clinical Data Management modernization.

Pursue Progress. Discover Extraordinary.
At Sanofi, we believe progress is made possible by diverse teams working together. Join us in embracing change, exploring new ideas, and discovering extraordinary opportunities. Let’s pursue progress together!

Sanofi is committed to diversity and inclusion. We provide equal opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch 'One Day at Sanofi' and learn more about our Diversity, Equity, and Inclusion initiatives at sanofi.com.