The RWE Evidence Synthesis Senior Associate is responsible for conducting systematic and targeted literature reviews, as well as scoping and rapid reviews that align with real-world evidence needs
Job Summary
The RWE Evidence Synthesis Senior Associate is responsible for conducting systematic and targeted literature reviews, as well as scoping and rapid reviews that align with real-world evidence needs.
Collaboration with statisticians is a key component, as you will translate results from indirect treatment comparisons (MAIC, STC) and network meta-analyses into clear, scientifically accurate reports and manuscripts.
Support cross-functional teams in HEOR and Medical Affairs by producing evidence summary slide decks and HTA-support documents.
Matching Summary
The RWE Evidence Synthesis Senior Associate is responsible for conducting systematic and targeted literature reviews, as well as scoping and rapid reviews that align with real-world evidence needs.
Skills & Requirements
Must-have
Systematic literature reviews
Real-world evidence needs
Draft research protocols
Data extraction and methodological descriptions
Technical narratives summarizing study designs
Indirect treatment comparisons (MAIC, STC)
Network meta-analyses
PRISMA, ISPOR, NICE, IQWiG standards
Nice-to-have
Strong communication skills
Organizational and project management abilities
Ability to function autonomously
Manage multiple priorities
Cross-functional collaboration
Key Requirements
Minimum 2 years hands-on experience in evidence synthesis
Experience working in Real-World Evidence (RWE) environments
Background in pharmaceutical, CRO, HEOR, or epidemiology settings
Previous experience with submissions to regulatory and/or core value dossier development
Good knowledge of technical guidelines (e.g., NICE, EU, HTA, IQWiG)
Competence with tools such as RevMan, GRADEpro
MSc or PhD in epidemiology, pharmacoepidemiology, public health, or life sciences field