IRT Manager - Clinical Supplies & IRT

Key Tasks & Responsibilities:
The IRT Manager assumes responsibility for operational execution of the IRT system used in clinical studies in development phases I to IV within clinical operations development operationsThe IRT is a critical system in ensuring safety of all patients taking investigational medicinal product (IMP,) and if not set-up correctly, could jeopardize the usability of data obtained within the clinical studies.As an expert in IRT, the Manager leads the set-up and testing of the system, ensuring it meets the requirements of the clinical study protocol and that all associated processes are fully compliant with GxP regulations.Revises / develops the clinical study protocol with particular focus on the attributes of study drugs including comparators, medical devices, randomization and blinding.Ensures appropriate supply of study medication for all patients in a clinical trial by implementing optimal IRT supply strategies.The Manager continues to assume accountability of the IRT during the systems life cycle, implementing all required amendments.Leads the IRT cross-functional sub-team and is accountable for the set-up and maintenance of the IRT System with special attention to the proper and correct supply of study sites with study medication, including the correct drug dispensation according to the study protocol.Responsible for providing guidance and training to study teams.Qualifications & Competencies:Bachelors Degree or equivalent. Pharmacist degree preferred5 to 8 years of relevant healthcare clinical development experienceProfound knowledge in drug developmentProfound knowledge in setting up Interactive Response (IRT) SystemsProfound knowledge in GCP and knowledge of GMPExcellent project management skillsExcellent communication skills (including fluent English).