Cta

As a Clinical Trial Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence..
**What you will be doing**:
- TMF filing, document quality checks, maintanance, compliance and oversight
- Development and delivery of site's ISF, assessment of eISF prior to SIVs
- maintain registries abd systems
- provide reporting to support management of studies
- support with audits and inspections readiness activities
- perform customisation and translation of documents
- manage archiving
- preparation of documents and communication for distribuition and collections from sites
**You are**:
- Bachelors degree/university degree
- Previous experience in clinical trials, ideally as a Clinical Trial Assistant
- Experience in clinical site payments would be an advantage
- Proven organizational and administrative skills.
- Computer proficiency
- Good knowledge of spoken and written ...