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Clinical Trials Manager
2 months ago
Job Summary:
i-Pharm Consulting is seeking a highly skilled Clinical Trial Manager to join our team. As a Clinical Trial Manager, you will be responsible for managing interventional clinical trials across Europe, ensuring all studies are executed in line with regulatory requirements and company guidelines.
Key Responsibilities:- Manage Clinical Studies: Oversee all components of small clinical studies, including Phase I trials, from initiation to close-out.
- Coordinate with Vendors: Work with Contract Research Organisations (CROs) and other vendors to ensure project deliverables are met.
- Develop Study Logistics: Develop and implement study logistics and plans to meet clinical study objectives.
- Monitor Progress: Provide oversight for site evaluations, initiation, routine monitoring visits, and study close-outs, ensuring all processes adhere to SOPs and regulatory requirements.
- Education: PharmD/PhD with 2+ years, MA/MS with 3+ years, or BA/BS/RN with 5+ years of relevant clinical or related experience in life sciences.
- Experience: Proven experience managing clinical trials in Europe, ideally with monitoring experience or strong country management skills.
- Skills: Advanced knowledge of study management, regulatory guidelines (FDA, EMA, ICH, GCP), and protocol requirements.
About the Role:
This is an excellent opportunity to contribute to a dynamic team within a leading pharmaceuticals company. If you are a proactive Clinical Trial Manager with strong experience in managing clinical trials within the EU, we would love to hear from you.
