Clinical Trials Senior Analyst
hace 4 semanas
Are you passionate about clinical trials and ensuring compliance with Mexican importation and exportation laws? We are looking for a Clinical Trials Senior Analyst to join our team at Novo Nordisk A/S in Mexico. If that sounds like you, read on to learn more about this exciting opportunity.
The Position
As a Clinical Trials Senior Analyst, you will be responsible for ensuring compliance with importation and exportation laws, maintaining close communication with CDC TMs, anticipating potential risks, and escalating any quality issues to the line manager. You will also be responsible for requesting necessary information from importers, following up on medicine and clinical supplies, and safeguarding company resources.
Qualifications
If you have a degree in Chemist Pharmacobiologist, Pharmaceutical Engineering, Biologist, or a similar field related to health science, and at least 3 years of experience as a Clinical Trials Assistant, preferably working with imports, with demonstrated skills in core competencies, then you could be the person we are looking for. You should also have knowledge of clinical trials imports and Mexican importation regulations, as well as advanced English proficiency.
About the Department
Our team in Mexico is responsible for running all clinical development activities from the initial planning of clinical trials towards authority submission. We investigate patients' reactions to new drugs, compare new drugs to existing products, and run a set of pre-specified trials in human beings. Our department provides Biostatistics and Programming, Clinical Reporting, Data Management, Epidemiology/Real World Evidence, and Clinical Pharmacology resources, processes, and competences to all development projects. We support all development projects by providing means for process alignment and optimisation, competency development, knowledge sharing, and training with regard to trial planning and execution.
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