RWE Epidemiologist & Study Lead

IQVIA; Turku; On-site; EUR 85,000 - 120,000; Full time

Job summary

IQVIA in Turku, Finland seeks an experienced epidemiologist to lead real-world evidence studies across early development to post-approval stages. You will collaborate with global clients and cross-functional teams, designing rigorous studies and ensuring scientific integrity and regulatory-aligned outcomes.

Responsibilities include protocol development, data strategy input, and leadership of smaller projects, with opportunities to contribute to client engagement and business development.

Qualifications

• Master's degree with 5+ years of relevant experience or PhD with 2+ years, in epidemiology/related field.
• Strong foundation in observational health research and real-world evidence generation.

Responsibilities

• Lead design, implementation, and execution of epidemiology methods for RWE studies across safety and effectiveness.
• Provide scientific and methodological support for research initiatives with senior team members.
• Serve as project lead for smaller studies and collaborate with senior project leaders.
• Develop and author study protocols, SAPs, and clinical study reports with high quality.
• Manage analyses and reporting, maintaining timelines and escalating risks as needed.
• Review analyses and provide input into SAPs, outputs, and interpretation of findings.
• Contribute to CRF/eCRF design, regulatory responses, and client-facing materials.
• Engage with clients to discuss study design, results, and progress with oversight as needed.

Skills

Epidemiology

Pharmacoepidemiology

Observational research

Real-world evidence

Study design

Statistical analysis

Client-facing

Regulatory knowledge

Education

Master's degree in Epidemiology/Pharmacoepidemiology/Public Health

PhD in Epidemiology/Pharmacoepidemiology/Public Health

Tools

SAS

R

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Edge

Job description

IQVIA in Turku, Finland seeks an experienced epidemiologist to lead real-world evidence studies across early development to post-approval stages. You will collaborate with global clients and cross-functional teams, designing rigorous studies and ensuring scientific integrity and regulatory-aligned outcomes.

Responsibilities include protocol development, data strategy input, and leadership of smaller projects, with opportunities to contribute to client engagement and business development.