Clinical Trial Manager

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.