INFECTIOUS DISEASE AND VACCINE CRO

Where disease spreads, we’re already there

Outbreak timing. Hard-to-reach populations. Safety at scale. AKEURA plans for them before the first participant enrolls, from Phase I vaccine trials through post-licensure effectiveness and safety studies.

Meet our experts

Vaccine development is in our blood

  • 400+

    infectious disease and vaccine studies

  • 40+

    vaccine targets across our portfolio

  • 500k+

    participants across 60+ countries

  • 100+

    studies in 10+ African countries

Deep infectious disease expertise,
pathogen by pathogen

Seasonality, transmission, and the settings where a disease circulates all change how a study should run. AKEURA’s infectious disease CRO services are planned around them, from vaccine development through real-world evidence.

Vaccines

From first dose to real-world effectiveness

Maternal, pediatric, adult, and older-adult vaccine studies, from Phase I through post-licensure

Our vaccine specialists cover dose and schedule selection, immunogenicity, efficacy, and safety, then follow through with effectiveness and burden-of-disease studies once your vaccine is licensed.

Respiratory infections

Seasons open fast and close faster

RSV, COVID-19, influenza, pneumococcal disease, pertussis, and human metapneumovirus

Our epidemiologists track disease burden and seasonality to put the right population in the right geography at the right time, so enrollment opens when the season does.

Tropical and vector-borne diseases

Endemic regions need local know-how

Malaria, dengue, chikungunya, Lyme disease, Japanese encephalitis, and yellow fever

Our own teams work where these diseases circulate, with site networks across Africa that know the local regulations, communities, and seasons before your study arrives.

Bacterial infections and resistance

Where antimicrobial resistance raises the stakes

Tuberculosis, meningococcal disease, E. coli, Group B strep, and cholera

From vaccine trials to studies of disease burden, we generate evidence on bacterial pathogens and drug-resistant strains across clinical and real-world settings.

Chronic viral infections

Evidence that keeps pace with chronic infection

HIV, viral hepatitis, HPV, herpes zoster, and other chronic and sexually transmitted infections

These studies often run for years. We plan follow-up and participant retention from the start, across clinical trials and real-world studies, so your data holds to the final visit.

Emerging and epidemic-prone diseases

Outbreaks don't wait for a perfect protocol

Lassa fever, Ebola, Zika, mpox, and other emerging and epidemic-prone threats

When an outbreak hits, timing is everything. Our epidemiologists and local teams build the incidence evidence that future vaccine studies depend on, before the next wave arrives.

Led by people who built their careers in vaccines

Meet the infectious disease and vaccine specialists behind your study.

Laurence De Moerlooze

Laurence De Moerlooze

Senior Vice President, Infectious Diseases and Vaccines

20+ years of sponsor-side vaccine development, from licensed vaccines to Zika, now leading infectious disease and vaccine programs.

Michael Katwere, MB ChB, MRCP(UK), MSc

Michael Katwere, MB ChB, MRCP(UK), MSc

Senior Medical Director

Practicing infectious disease physician with 15+ years in pharmacovigilance and trials, from Ebola to HIV vaccines.

Edward Sobe Yarig, MSc

Edward Sobe Yarig, MSc

Director, Project Strategy and Delivery, Infectious Diseases and Vaccines

18+ years leading clinical operations across Sub-Saharan Africa, from Ebola and Lassa fever to tuberculosis and malaria.

Kaatje Bollaerts

Kaatje Bollaerts

Senior Vice President, Real-World Evidence

20+ years in vaccine and infectious disease biostatistics, now leading global real-world evidence research and partnerships.

Direct access to deep expertise

Laurence De Moerlooze

Global Head of Infectious Diseases and Vaccines

[Short bio to come.]

Edward Sobe Yarig

Pneumococcal and Meningococcal Vaccine Evidence
[Short bio to come.]

Adriana Bastidas

Medical Monitoring and Vaccine Safety
[Short bio to come.]

Kaatje Bollaerts

Global Head of Real-World Evidence
Co-editor of Vaccination Programmes: Epidemiology, Monitoring, and Evaluation

Bradford Gessner

Position

[Short bio to come.]

Ola Polkowska-Kramek

Position

[Short bio to come.]

In-house scientific experts

Our medical monitors, epidemiologists, and therapeutic-area specialists are in protocol design meetings, on safety calls, and on the paper when the results publish.

Aleksandra Polkowska-Kramek, PhD

Aleksandra Polkowska-Kramek, PhD

Program Head, Epidemiology

Leading infectious disease and vaccine evidence programs, backed by 10+ years of epidemiology and public health work.

Emeka (Chukwuemeka) Onwuchekwa, MBBS, MSc, MPH

Emeka (Chukwuemeka) Onwuchekwa, MBBS, MSc, MPH

Senior Epidemiologist

Leading observational studies in RSV and pneumococcal disease, drawing on deep US and European real-world data expertise.

Elisabeth (Lisanne) Mesfun-Kap, MSc

Elisabeth (Lisanne) Mesfun-Kap, MSc

Head of Epidemiology

7+ years of real-world evidence across oncology, heart failure, and liver disease, now leading epidemiological study design for vaccine research.

Margarita Riera, MD, MSc

Margarita Riera, MD, MSc

Strategy Director, Real-World Evidence

Field medicine and epidemiology across Africa and Asia, now shaping real-world evidence strategy for vaccine research.

Omar Okasha, MD, MPH

Omar Okasha, MD, MPH

Epidemiologist

Leading real-world studies of vaccine impact, effectiveness, and safety, backed by 20+ years as a physician-epidemiologist.

Jennifer Eeuwijk, MSc

Jennifer Eeuwijk, MSc

Senior Epidemiologist

15+ years in epidemiology and evidence synthesis, now leading systematic reviews across infectious diseases and vaccines.

Outbreaks move fast. So do we.

Incidence shifts. Seasons close. Infrastructure varies.

Our studies are led by senior experts who built their careers inside vaccine development.

1

Infectious disease moves before the recruitment plan does.

Our approach

Our epidemiologists map disease burden, seasonality, and eligible populations long before site selection, so decisions rest on evidence, not optimism.

Our epidemiologists have run 145+ vaccine real-world evidence studies, so they know where your participants are before the first site opens.

2

A global protocol still has to work on the ground.

Our approach

Local teams and proven sites lead, with regional experts guiding local regulations, logistics, community engagement, and study quality in Africa and other low-resource settings.

We’ve been running studies in Africa for 25 years, long before it showed up on anyone’s strategy slide.

3

Big programs need big reach.

Our approach

We build real relationships with sites in the most challenging geographies, so enrollment holds across countries and seasons.

Our Primary Care Research Network gives you direct access to hundreds of primary care practitioners, pharmacists, and practice assistants.

4

Vaccine safety at scale, without the bureaucracy.

Our approach

Pharmacovigilance specialists sit inside the study team, so medical monitoring, safety oversight, and regulatory reporting scale from a first-dose study to a full vaccine portfolio.

What started as a single-study project became a 15-year partnership spanning more than 20 vaccine studies across four regions.

5

Licensure answers one question. RWE answers the rest.

Our approach

Specialized clinical and real-world evidence teams plan together early, so the evidence your vaccine needs after licensure is designed before you need it.

Behind that are 160+ clinical and 210+ real-world infectious disease studies.

6

The team that pitched isn’t the team that runs it.

Our approach

Not here. Your named experts stay with your study from protocol to final report.

The expert who writes your protocol signs off your final report. Same name, same number, start to finish.

Evidence from the field

White papers, fact sheets, and case studies from our infectious disease and vaccine teams.

Discover more infectious disease and vaccine insights
White paper

Research at the speed of outbreak

With more than 1,000 confirmed cases and no licensed Bundibugyo-specific vaccine, the race to generate evidence is already on. Our experts share what past Ebola trials got right and how sponsors, regulators, and communities can move faster without compromising safety, ethics, or trust. Download the white paper for practical recommendations to start studies faster in outbreak settings.

Fact sheet

Vaccine development is in our blood

Our teams bring 25+ years of vaccine research across 40+ targets, from respiratory viruses and tuberculosis to tropical and emerging diseases. With 400+ studies, 500,000+ participants, and our own teams on the ground across Africa, we know the pathogen, the populations, and the places where disease circulates. Download the fact sheet to see how we support programs from Phase I through post-licensure.

Case study

Some partnerships last a study. Ours lasted a vaccine program.

Over 15 years, we grew from a functional service provider to a full-service partner, managing 10+ active studies at once without losing speed. When a new regulatory requirement came up mid-trial, our senior experts modified the protocol within days. Download the case study to see how we helped a mid-size biotech reach licensure.

Support at every stage of development

Early phase clinical development

Confident first steps from first dose to proof of concept, with answers your next study can trust

Late phase clinical development

Phase IIb to Phase IV trials at scale, built to carry your program through approval and beyond

Real-world evidence studies

Regulatory-grade post-approval safety and effectiveness studies, led by RWE specialists who stay within reach

Frequently asked questions

Answers to your questions about our infectious disease and vaccine expertise

An infectious disease and vaccine CRO designs and runs clinical trials and real-world evidence studies for vaccines and infectious disease treatments. AKEURA is a specialist infectious disease and vaccine CRO with 400+ studies across 60+ countries, from first-in-human studies through Phase IV and real-world evidence.

AKEURA runs Phase I–IV vaccine clinical trials, including first-in-human, dose and schedule selection, immunogenicity, efficacy, safety, and post-licensure studies. We also run standalone real-world evidence studies.

AKEURA’s experience includes RSV, COVID-19, influenza, pneumococcal disease, tuberculosis, HIV, hepatitis, HPV, herpes zoster, Lyme disease, chikungunya, dengue, malaria, polio, Zika, Ebola, and Lassa fever, as well as other viral and bacterial diseases.

Yes. AKEURA has delivered 100+ studies in more than 10 African countries. Our local teams and site relationships support the full study lifecycle from the ground in diverse and low-resource settings.

Cultural, regulatory, and infrastructure differences vary country by country across Africa, and so do health-seeking behaviors and ethics review. AKEURA’s local teams plan for each from the start, so your study is built for the setting rather than adapted to it.

Yes. AKEURA runs vaccine studies in maternal, pediatric, adult, and older-adult populations. Our scientific advisors and infectious disease and vaccine study leaders deliver support built around the population and the study. No need for templates.

AKEURA runs vaccine effectiveness, safety, burden-of-disease, utilization, and treatment-pattern studies. Designs include registries, database and electronic health record analyses, prospective observational studies, and collaborative evidence networks.

AKEURA provides medical monitoring, case handling, signal detection, safety database support, aggregate and regulatory reporting, and reconciliation. Pharmacovigilance teams can work within your procedures or ours, from one first-in-human study to a full vaccine portfolio.

AKEURA maps disease burden with treatment patterns and eligible populations, as well as regulatory timelines and site readiness. We prepare long before activation. Countries and sites are chosen specifically for this protocol and this enrollment window, not because they worked last time.

Look for vaccine-specific medical and operational experience and proven access to sites in the geographies you need with direct access to the study leaders before and after approval. Ask who will actually run the study. Then make sure those people stay.

Connect with an expert

Tell us what you need.
Your message goes to the team that handles your study.

Name
Laurence De Moerlooze

Laurence De Moerlooze

Senior Vice President, Infectious Diseases and Vaccines

20+ years of sponsor-side vaccine development, from licensed vaccines to Zika, now leading infectious disease and vaccine programs.