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, Flexible
* Location: Ireland, Remote
* Contract Type: Permanent, Full Time
* Language: English
* Project: Various Therapeutic Areas
Key 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.