Life Sciences BA & R&D Data Specialist (Hybrid)

Migx; Barcelona; Hybrid; EUR 50,000 - 80,000; Full time

Benefits offered by this job

Hybrid work model in Barcelona

Excellent compensation package

Social benefits package

Career development opportunities

Friendly atmosphere

Job summary

MIGx, a global healthcare and life sciences consulting firm, seeks a Mid-Senior Life Sciences Consultant/Business Analyst to join its Barcelona team. You will drive digital transformation and data excellence in pharma R&D, collaborating with global teams on regulatory and GxP projects.

The role emphasizes cross-functional collaboration, data modeling and system integration with a focus on drug development and CMC initiatives in a fast-growing, international environment.

Qualifications

• Experience with drug development lifecycle and regulatory requirements.
• Subject matter expert in Pharmaceutical R&D or CMC.
• Experience with data modeling, requirements engineering, and process mapping.
• Familiarity with Pharma R&D systems (CDMS, CTMS, PV, RIM, LIMS, ELN, eTMF).

Responsibilities

• Work with cross-functional teams to gather and analyze business requirements.
• Create technical specifications and other documentation.
• Analyze and model complex process/data flows to support pharmaceutical R&D or CMC initiatives.
• Support system implementation, integration, data quality initiatives and validation efforts.
• Participate in requirement workshops and User Acceptance Testing.
• Use subject matter expertise to support and guide internal teams.
• Act as trusted advisor to clients on digital transformation in life sciences.
• Participate in workshops, gap analyses, and process improvements.

Skills

Data visualization

Requirements gathering

Process mapping

Stakeholder engagement

Tools

Power BI

Tableau

Spotfire

Job description

MIGx, a global healthcare and life sciences consulting firm, seeks a Mid-Senior Life Sciences Consultant/Business Analyst to join its Barcelona team. You will drive digital transformation and data excellence in pharma R&D, collaborating with global teams on regulatory and GxP projects.

The role emphasizes cross-functional collaboration, data modeling and system integration with a focus on drug development and CMC initiatives in a fast-growing, international environment.