Backed by GV and SoftBank VF.
About the role
You will be responsible for overseeing the supply chain operations for clinical trials, including the management of investigational medicinal products (IMPs) and comparators. This role will be pivotal in ensuring that study sites are supplied with the necessary products on time and in full compliance with regulatory requirements. The ideal candidate will have a strong analytical, organizational, and communication skill set, with the ability to manage multiple tasks in a dynamic, fast-paced environment. Found on 1752vc Careers, the job board for startup and VC roles.
More about this role
You will be responsible for overseeing the supply chain operations for clinical trials, including the management of investigational medicinal products (IMPs) and comparators. This role will be pivotal in ensuring that study sites are supplied with the necessary products on time and in full compliance with regulatory requirements. The ideal candidate will have a strong analytical, organizational, and communication skill set, with the ability to manage multiple tasks in a dynamic, fast-paced environment.
· Monitor IP inventory levels at depots and clinical trial sites to proactively manage supply chain risks and prevent any interruptions to study timelines.
· Coordinate the import, export, and transportation of clinical trial materials (CTM) to ensure timely delivery and compliance with regulatory requirements.
· Track shipments to and from clinical sites, ensuring adherence to timelines and quality standards.
· Support Author development and approval of English label text for investigational drugs, translations, and approval of final label design while ensuring compliance with regulatory and quality standards.
· Oversee the packaging and labeling processes at clinical supply...
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