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.

Clean laboratory glassware arranged on a bench
  • 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.

A dark analytics dashboard showing several line and bar charts
  • 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.