Offer summary
Qualifications:
Bachelor's Degree, Proficiency in MS Outlook, Word, Excel, PowerPoint, Basic understanding of study-related documentation, eTMF (Veeva) experience preferred, Ability to work with global teams.
Key responsabilities:
- Support all phases of clinical studies under supervision
- Plan and communicate clinical study timelines
- Oversee operational aspects of clinical trials
- Assist with the creation and management of project trackers
- Act as point of contact for designated projects