Job Type:12 month(Fixed Term Contract) Location: Cork/Dublin Work Model:Hybrid (1 - 2 days onsite at Customer Site in Cork per month with occasional travel to Dublin as per business needs). Description Document Development and Writing: Author, review, and finalisehigh-quality clinical trial documents, including but not limited to: Study Protocols and Protocol Amendments: Develop comprehensive and scientifically rigorous protocols that align with regulatory and ethical standards. […]
Regulatory Compliance and Quality Assurance: Ensure all documents comply withICH GCP, regulatory requirements, and...