Associate Clinical Trial Manager – Neuroscience & Ophthalmology

Medpace; Cincinnati (OH); Presencial; GBP 42 000 - 70 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored events

Employee health and wellness

Resumo da oferta

Medpace is seeking an Associate Clinical Trial Manager (aCTM) for a full-time, office-based role in the Clinical Trial Management team. The position targets candidates with PhDs or post-doctoral research experience seeking to apply analytical and academic skills to clinical project administration.

Responsibilities include collaboration with project coordinators, timely delivery of tasks, maintaining status reports, interacting with sponsors and sites, QC of regulatory filings, study supplies

Qualificações

• PhD in Life Sciences is required.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced international team.
• Prior CRO or pharmaceutical industry experience is not required but advantageous.

Responsabilidades

• 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 CTMS.
• Interact with internal project team, Sponsor, study sites, and third-party vendors.
• Manage and perform quality control of our internal regulatory filing system.
• Provide oversight and management of study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Conhecimentos

English fluency

Analytical skills

Communication

Team collaboration

Formação académica

PhD in Life Sciences

Descrição da oferta de emprego

Medpace is seeking an Associate Clinical Trial Manager (aCTM) for a full-time, office-based role in the Clinical Trial Management team. The position targets candidates with PhDs or post-doctoral research experience seeking to apply analytical and academic skills to clinical project administration.

Responsibilities include collaboration with project coordinators, timely delivery of tasks, maintaining status reports, interacting with sponsors and sites, QC of regulatory filings, study supplies