Services
Study design through to published results.
A full-service CRO built on epidemiological and scientific expertise, spanning more than thirty years and a wide range of therapeutic areas, among them oncology, orthopaedics, infectious diseases and immunology.
01
Clinical trials
Interventional and observational research across every phase, with remote and risk-based monitoring and partnerships with top-tier hospital sites and research centres globally.

- Phase I-III trials
- Phase IV, post-approval
- Post-Marketing Observational Studies (PMOS)
- Real World Evidence (RWE)
- Chart review, registries, database analysis and epidemiological surveys
- Medical devices
02
Market access and HEOR
Health economics and outcomes research, added to our capability in 2012, built to carry a product through to reimbursement.
- Literature reviews
- Medical writing, including pharmacoeconomic reports and medical summaries
- Budget impact analysis
- Cost-effectiveness models
- Graphical user interface platforms
- Reimbursement submission preparation
- Validation sessions and panel meetings
03
Biostatistics and medical writing
Our scientific core. Over 150 manuscripts published by the JSS team, at a 90% acceptance rate.

- Analysis dataset generation
- Tables, figures and listings development
- Sample size calculations
- Advanced biostatistics: multivariate analysis, PK/PD, simulation
- CDISC SDTM and ADaM mapping
- SAS macro development
- Rescue analysis
04
Consulting
Strategic advice and training, from a clinical development plan at the outset to an audit at the end.
- Clinical development plans and strategic assessments
- Study design and protocol development
- Regulatory consulting
- Investigator-initiated studies
- QA services, compliance, SOP development and auditing
- Risk management and patient reported outcomes
- Training courses in statistics, clinical research architecture and health economics
05
Insourcing
Sometimes the right answer is not a vendor but a person in your own team. We place qualified personnel and project managers on in-sourcing mandates for as long as the work requires.
- Personnel qualified in ICH and GCP
- Therapeutic area expertise
- Pharmacovigilance
- Project managers
- In-sourcing mandates
Ready to talk about your next study?
Tell us where you are in development and we will tell you, honestly, whether we are the right CRO for it.
+1 514-934-6116 · +1 866-934-6116 toll free