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.
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