JOHESE Clinical research will be responsible for the following during the clinical trial process:

  • Feasibilities
  • Get the necessary PI / Sub Investigators on board for the study
  • Collect CV’s and other documents from the Investigators
  • Contracts will be handled by JOHESE
  • Training of staff (with the help of the PI)
  • Recruitment of patients
  • Perform normal SSC functions at the site that includes the patient tests/vitals ect.
  • Process all data
  • Control all Investigator Products
  • Assist CRO / CRA / Sponsor
  • Be the link between the Investigator / Patient and the CRO to provide quality data with quality patients.

We specialises in the following therapeutic areas:

  • Cardiology
  • Diabetes
  • Oncology
  • Endocrinology
  • Internal diseases
  • Physiotherapy / Pain Medication
  • UTI
  • Influenza / Flu
  • Pulmonology (Asthma and COPD)
  • ICU studies
  • Gastroenterology