Description
We are seeking a motivated, passionate and enthusiastic clinical trials professional to join our team in Sofia, Bulgaria.
As a Clinical Trials Professional, you will perform daily administrative activities to ensure a complete and accurate Trial Master File (TMF) delivery.
Essential Functions
- Assist local project team members with accurately updating and maintaining clinical documents and systems (Trial Master File) within project and company timelines.
- Assist the clinical team with the handling, filing and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist the clinical team with site visit preparation by identifying and sharing missing documents for TMF.
- Act as a central contact for the clinical team for TMF and associated documentation (including TMF set-up, periodic review, Action Item resolution).
Candidate Profile
- Education: Bachelor’s degree (life sciences preferred); candidates pursuing a Bachelor’s degree are also welcome to apply, if available for full-time employment.
- Experience: both candidates with limited/no experience and professionals can be considered. Admin experience is a plus.
- Good computer skills: processing large amounts of data in Excel (ideally, including basic formulas), experience of working with databases or trackers/tables. Knowledge of TMF a big plus, but not required.
- Detail-oriented: attention to detail, ability to focus on routine and prolonged tasks.
- Fluent in English.
- Work model: hybrid preferred. 1 month in the office preferred for onboarding.
At IQVIA, you will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there!