In this full-time, office-based role you join the Clinical Trial Management team as an aCTM, applying your PhD or postdoctoral experience to support global clinical trials. You will collaborate with Project Coordinators and Clinical Trial Managers to deliver study activities with high accuracy. The position offers intensive training, international exposure, and a clear path toward leadership in CTM. This is an opportunity to translate rigorous research skills into practical trial management impact.
Retribuzione / Benefits
- Collaborate on global study activities with project team and sponsors
- Ensure timely delivery of recurrent tasks with high accuracy
- Compile and maintain project-specific status reports in the CTM system
- Interact with internal project team, Sponsor, study sites, and third-party vendors
- Manage and perform quality control of the internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
Responsabilità
- PhD in Life Sciences
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced, international team
- Prior CRO or pharmaceutical industry experience is advantageous but not required
Requisiti fondamentali
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.