Business Analyst - Pharmaceutical Global Regulatory Affairs AND Data ESSENTIAL - FULL REMOTE

Project overview

Business Analyst – Pharmaceutical Global Regulatory Affairs AND Data/health or clinical data standards 3 to 6 years or more of experience as a Business Analyst in data, health, or regulatory contexts.

Daily rate 500 Euro less than 10 years exp/575 Euro max more than 10 years exp.

Clinical and operational data Required skills

A Business Analyst to support initiatives involving clinical and operational data (MDM, SSU, CTMS, Site Connect, CRM, supply chain, finance, ERP).

The consultant will act as the interface between business stakeholders, clinical teams, and data/engineering teams, in order to translate business needs into actionable data requirements.

Main responsibilities

Profile sought

Work environment

• Solid experience with health/clinical data standards (HL7, FHIR, ICD-10, LOINC, etc.).
• Good understanding of data platforms and pipelines (Snowflake, dbt, IICS appreciated).
• Ability to write clear functional documentation, user stories, and acceptance criteria.
• Excellent communication skills and experience in an Agile environment.
• 3 to 6 years or more of experience as a Business Analyst in data, health, or regulatory contexts.
• Collect, analyze, and document business needs related to clinical and operational data use cases.
• Translate functional needs into clear specifications for data engineering and analytics teams.
• Contribute to data quality, traceability (data lineage), and governance activities (definitions, data dictionaries, validation rules).
• Lead workshops with clinical and operational stakeholders and ensure alignment between teams.
• Contribute to backlog management and sprint planning via Jira; document processes in Confluence.

Project details

• Start: ASAP
• Duration: 3 mois renouvelable
• Remote: remote
• Location: Paris, France, FR
• Rate: 50-71 EUR/h
• Languages: French