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We are seeking a highly skilled Clinical Trial Manager with expertise in Neuroscience to join our team in Spain. As a key member of our Clinical Trial Management Group, you will be responsible for managing and providing accountability for day-to-day operations of clinical trials, ensuring compliance with ICH/GCP and all applicable laws, rules, and regulations.
Key Responsibilities- Manage and provide accountability for day-to-day operations of clinical trials
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in-depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report
- Develop operational project plans
- Manage risk assessment and execution
- Responsible for management of study vendor
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
- Bachelor's degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred
- Experience in Phases 1-4; Phases 2-3 preferred
- Minimum of 2 years of Clinical Trial Management experience; CRO experience preferred; 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role
- Strong leadership skills
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
