- Bulgaria
- Full-time · Entry
- 0–2 years
Provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.
Responsibilities
- Support the clinical team’s inhouse activities on assigned projects
- Co-ordinate and maintain clinical study documentation in the Trial Master Files (TMF)
- Support the clinical team in essential document development, collection and management process
- Manage the Clinical Trial Management System (CTMS)
- Create the Investigator Site Files, co-ordinating the ordering, dispatch and tracking of trial materials
Requirements
- Relevant experience/qualifications in Life Sciences or related field or administration
- Nice to have: Pharmaceutical industry experience
- Nice to have: CRO experience
- Nice to have: Healthcare industry experience