Job Description
Responsibilities:
- Guide and support research staff on GCP/ICH compliance and study protocols.
- Lead, mentor, and coordinate study coordinators and assistants to execute trial activities effectively.
- Monitor study tools, metrics, and deliverables to ensure high-quality results.
Requirements:
- Extensive experience as a Study Coordinator in clinical research.
- Strong knowledge of ICH/GCP guidelines and regulatory requirements.
- Proficiency in applying SOPs and global clinical research standards.
Qualities:
- Highly organized with the ability to multitask and work independently or collaboratively.
- Excellent communication skills and a proactive, solution-oriented mindset.
- Flexibility to operate across multiple European locations remotely.
About Jobgether
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