EPM Scientific are currently partnered with a small CRO running multiple projects. They are urgently seeking a Clinical Trial Manager to support their expanding clinical operations team. See a short summary below:Role Overview:Ideal Start date: December, FlexibleLocation: Ireland, RemoteContract Type: Permanent, Full TimeLanguage: EnglishProject: Various Therapeutic AreasKey Responsibilities:Oversee and manage all aspects of assigned clinical trials from start-up to close-out.Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs.Coordinate with CROs, vendors, and internal stakeholders to ensure timely and high-quality deliverables.Manage trial timelines, budgets, and risk mitigation strategies.Prepare and review essential documents for regulatory submissions and ethics approvals.Monitor trial progress and provide regular updates to senior management.Troubleshoot operational issues and implement corrective actions as needed.Requirements:Bachelor's or Master's degree in Life Sciences or related field.Strong experience in clinical trial management (3+ years preferred).Proven track record in managing global trials; oncology experience highly desirable.Excellent knowledge of ICH-GCP and regulatory guidelines.Strong organizational, communication, and problem-solving skills.Ability to work independently in a remote setting and manage multiple priorities.If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.