Data Analytics Expert for Pharmacovigilance (all genders) - full-time/part-time

Merck Group; Deutschland; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

An international pharmaceutical company is seeking a Senior Data & Technology Manager in Germany. The role focuses on Safety Data Retrieval & Analysis, leveraging expertise in commercial pharmacovigilance systems. You will maintain safety data warehouses, oversee validation activities, and translate scientific questions. Ideal candidates have a degree in Data Science or related fields, with five years of experience in BI tools and pharmacovigilance knowledge. Strong stakeholder communication and project management skills are crucial.

Qualifikationen

• Approximately five years of relevant working experience with BI/reporting tools.
• Proven pharmacovigilance knowledge and experience with drug safety systems.
• Fluent in English; proficiency in German is a plus.

Aufgaben

• Maintain the validated state of the ArisGlobal commercial safety data warehouse.
• Collaborate with the Qualified Person for Pharmacovigilance for data retrieval.
• Translate medical and scientific questions into technical solutions.

Kenntnisse

Python

Tableau

SQL

Cognos

Snowflake

Excellent stakeholder communication

Ausbildung

University degree in Data Science, Bioinformatics, Biostatistics, Computer Science, or Life Sciences

Tools

HP ALM

Jobbeschreibung

Overview

Your role: We are seeking a Senior Data & Technology Manager to focus on Safety Data Retrieval & Analysis while partnering with Regulatory Data Retrieval & Analytics. In this role, you will leverage your expertise in commercial pharmacovigilance (PV) systems and your strong knowledge of pharmacovigilance to drive the retrieval, analysis, and visualization of complex data. Your expertise will enable you to design, implement, and promote novel advanced analytical tools, building the next generation of safety capabilities by delivering value adding benefit risk information.

Key Responsibilities

• Maintain the validated state of the ArisGlobal commercial safety data warehouse (AWS/Snowflake).
• Verify changes to reports through testing in non-production environments.
• Oversee validation activities for new releases or change controls in compliance with GxP regulations.
• Prepare for and support health authority audits and inspections.
• Collaborate with the Qualified Person for Pharmacovigilance and her team to retrieve data from the safety database, ensuring compliant, high-quality analyses for Global Patient Safety.
• Translate medical and scientific questions into robust technical solutions and act as the interface between operations, medical, and IT teams.
• Specify and develop complex reports and dashboards using tools such as Snowflake, IBM Cognos, Python, and Tableau.
• Drive continuous improvement and explore advanced technologies, including Snowflake features and knowledge graphs.

Who you are

• University degree in Data Science, Bioinformatics, Biostatistics, Computer Science, or Life Sciences.
• Approximately five years of relevant working experience, particularly with BI/reporting tools and technologies (e.g., Python, Tableau, SQL, Cognos, Snowflake). Experience with knowledge graphs is a plus.
• Proven pharmacovigilance knowledge and experience with commercial drug safety systems.
• Strong sense of accountability and ownership, with a capacity for rapid learning.
• Excellent project and vendor management skills.
• Knowledge of GxP/GVP regulations and experience with test/validation management (HP ALM) of computerized systems.
• Fluent in English; proficiency in German is a plus.
• Excellent stakeholder communication skills, with the ability to translate scientific questions into technical requirements.
• Ability to manage multiple projects simultaneously in a structured manner and build strong relationships within interdisciplinary teams.