Statements (46)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
Job Role
|
| gptkbp:advises |
Regulatory changes
|
| gptkbp:analyzes |
Study data
|
| gptkbp:assists |
Study design
Budget negotiations |
| gptkbp:associatedWith |
Investigational sites
|
| gptkbp:collaboratesWith |
Investigators
|
| gptkbp:communicationEquipment |
Sponsors
|
| gptkbp:communityFeedback |
Study teams
|
| gptkbp:compatibleWith |
Good Clinical Practice (GCP)
|
| gptkbp:conducts |
Site visits
Site initiation visits Ensure protocol adherence |
| gptkbp:conductsResearchOn |
Trial progress
|
| gptkbp:coordinatesWith |
Laboratories
|
| gptkbp:develops |
Monitoring plans
|
| gptkbp:developsStrategiesFor |
Study documentation
|
| gptkbp:ensures |
Data entry
Regulatory requirements |
| gptkbp:evaluates |
Site performance
Adverse events |
| gptkbp:facilitates |
Patient recruitment
|
| gptkbp:hasSustainabilityInitiatives |
Data collection
|
| https://www.w3.org/2000/01/rdf-schema#label |
Clinical Research Associate
|
| gptkbp:maintains |
Trial activities
|
| gptkbp:manages |
Study timelines
|
| gptkbp:monitors |
Data integrity
|
| gptkbp:operates |
Clinical_Research_Manager
|
| gptkbp:participatesIn |
Site selection
Audit preparations Data monitoring committees |
| gptkbp:provides |
Clinical trial participants
|
| gptkbp:providesInformationOn |
Study design changes
|
| gptkbp:providesSupportFor |
Regulatory submissions
|
| gptkbp:providesTrainingFor |
New staff
Site staff |
| gptkbp:recognizes |
Potential issues
|
| gptkbp:responsibleFor |
Monitoring clinical trials
|
| gptkbp:reviews |
Feasibility
Informed consent forms |
| gptkbp:supports |
Patient safety initiatives
|
| gptkbp:track |
Study budgets
|
| gptkbp:updates |
Stakeholders
|
| gptkbp:utilizes |
Clinical trial management systems
|
| gptkbp:visitedBy |
Project meetings
|
| gptkbp:worksWith |
Clinical trial sites
|