Clinical Trials Unit

Nursing tasks charged to funded projects:

1. Study Coordination:

  • Collection of signatures for the study documents and delivery to the promoter
  • Intermediary between research team and CRO
  • Investigator file management
  • Organization of the start-up meeting
  • Coordination of monitoring visits
  • Coordination of visits of patients according to protocol with the family and the rest of internal actors (services for complementary tests, etc.)

2. Nursing tasks:

  • Taking of constants, weight and size
  • Perform ECG
  • Record of adverse events
  • Follow-up of the patient's condition
  • Record of concomitant medication
  • Study Medication Counts and Adherence Calculation
  • Dispensation of the study drug and return to the pharmacy service
  • Education of study drug administration
  • Questionnaires
  • Make and schedule analytic requests
  • Blood extraction
  • Sample Processing
  • Dry ice management
  • Send samples to external laboratories
  • Registration and storage of frozen samples
  • Maintenance of laboratory kits
  • Record of data in the medical record
  • Management of patient expenses

3. Data entry:

  • Data entry in the CRD s in the period established by protocol
  • Resolution of queries
  • Review of patient stories with or without the monitor
  • Monitoring

Service Fees

Contact with:

Mrs Joana Claverol Torres
Coordinator of the Clinical Trials Unit
coordinador.URC@fsjd.org


More information about the Clinical Trials Unit