In this role you drive day-to-day trial operations within Medpace’s Clinical Trial Management Group in Madrid, leveraging CNS/Ophthalmology expertise to advance therapeutic development. You will partner with cross-functional teams to ensure study deliverables meet ICH/GCP standards and contractual obligations, while guiding risk management and vendor oversight.
You help shape operational plans and sponsor communications, contributing to patient-centered outcomes. This position offers remote flexibility after probation and a path to leadership within a general CRO.
Compensaciones / Beneficios
- Manage day-to-day project operations per contract and ICH/GCP requirements
- Serve as primary Sponsor contact for operational issues and study deliverables
- Maintain in-depth knowledge of protocol, therapeutic area, and indication
- Oversee cross-functional project teams and ensure training compliance
- Review input for study protocol, edit check specs, data analysis plan, and final study report when applicable
- Develop operational project plans and manage risk assessment and execution
- Oversee management of study vendors
- Ensure site quality and supervise Clinical Research Associates and monitoring deliverables
Responsabilidades
- Bachelor's degree in a health or life science-related field
- Two years minimum Clinical Trial Management experience; CRO experience preferred
- Experience in Phases 1-4 (Phases 2-3 preferred)
- CRO experience preferred; strong leadership skills; bid defense experience preferred
- Experience in managing overall project timelines
- Experience with CNS/Ophthalmology therapeutic areas (desirable)
Requisitos principales
- competitive salary/bonus program
- equity grants
- comprehensive health, wellness, retirement, and PTO benefits
- office-based culture with occasional WFH after training
- on-site mentors and defined career paths
- continuous training and development opportunities