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GCP Guidelines Compliance Specialist
hace 2 semanas
Fortrea is seeking a highly skilled GCP Guidelines Compliance Specialist to join our team. As a key member of our documentation team, you will be responsible for ensuring compliance with GCP guidelines and regulatory requirements.
You will apply your knowledge to review and develop Informed Consent Forms (ICF) that meet global industry standards.
Your primary responsibilities will include:
- Developing and reviewing clinical trial documents, including informed consent forms;
- Applying knowledge of GCP guidelines and regulatory requirements to ensure compliance;
- Liaising with project managers to communicate trends, outstanding issues, and safety concerns;
- Supporting the development, review, and approval of master templates;
- Creating, reviewing, and revising training materials and plans;
To succeed in this role, you should possess excellent communication and customer service skills, as well as the ability to influence stakeholders through insight into industry trends.