Sanofi Data Analyst Job For Life Sciences, Apply Online
Data Standards Analyst
Hyderabad, India
Permanent
Posted on: Jan. 17, 2025
Closing on: Mar. 05, 2025
The Data Standards Analyst represents Sanofi in all internal & external networks initiatives (CDISC, TransCelerate, etc.), monitors actively Health Authorities requirements, and promotes Data Standards knowledge and best practices within Sanofi. At the study level, the Data Standards Analyst supports clinical teams and Standards leads during the review of study-specific metadata based on customer needs and provides effective input through regular analysis of information reported from a broad variety of sources.
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Clinical Information Governance team as Data Standards Analyst, and you’ll help shape the future of Clinical Data Standards at Sanofi and across our industry.
Main responsibilities:
- Supports the Metadata Leads for CDASH, SDTM, External Data, or Controlled Terminology.
- Understands the application of the CDISC models across the life cycle of a trial.
- Contributes to the support of Global/Study Request Review Meetings for the specific Data Standards Model of expertise.
- Provides input during the eCRF review (study level) with the Study Team and ensures study-specific metadata are aligned with the CIG Clinical Data Standards strategy.
- Reviews study requests (Data Collection, External Data, Controlled Terminology, or SDTM).
- Contributes to developing CDISC-compliant end-to-end metadata specifications for new study-specific forms.
- Supports Clinical Data Standard Leaders with the management of global requests (review/meeting/implementation in Sanofi Metadata/metadata QC/standard documentation updates).
- Participates in Core and TA standard needs definition (SDTM and TA WG).
- Contributes to Global governance process definition and/or optimization.
- Monitors study-specific forms developed with Standard potential at the Therapeutic Area level.
About you
Experience:
- Experience in the Pharmaceutical Industry, with strong involvement in the “clinical data flow,” specialized in Data Standards Management.
- Good knowledge of industry data standards and practices (e.g., CDISC/CDASH/SDTM).
- Good understanding of CDISC and Metadata Governance practices (Preferred CDISC certification in one or more of the models).
- Familiar with end-to-end clinical data flows and data structures.
Soft and technical skills:
- Strong English skills (verbal and written), ability to exchange fluently in a global environment. Efficient communication skills and good organization skills.
- Ability to negotiate and gain acceptance of others. Ability to coordinate/oversee multiple tasks simultaneously. Project team collaboration by interacting with internal or external partners in/outside the Department and with their leaders. Self-motivated & results driven with attention to detail and quality.
Education: Bachelor’s degree or above, preferably in Life Science or related field.
Languages: Excellent English language knowledge – written and spoken.
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