Descrizione dell'offerta
Experteer Overview
In this role you will support Medpace’s Clinical Trial Management team as an Associate Clinical Trial Manager. You will work with Project Coordinators and Clinical Trial Managers to drive clinical trial activities and ensure timely, accurate deliverables. This position offers intensive training, an international environment, and a pathway into clinical trial management. You will contribute to the administration and oversight of trials that advance cutting‑edge therapeutics, shaping processes and timelines. This is a chance to apply your analytical background in a fast‑paced setting with meaningful impact.
Retribuzione / Benefits
- Communicate and collaborate on global study activities with project coordinators and clinical trial managers
- Ensure timely delivery of recurrent tasks with high accuracy
- Compile and maintain project‑specific status reports in the clinical trial management system
- Interact with internal project team, Sponsor, study sites, and third‑party vendors
- Manage and perform quality control of 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 dynamic industry within an international team
- Prior CRO or pharmaceutical industry experience not required but advantageous
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
Candidatura e Ritorno (in fondo)
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