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Clinical Trials Senior Analyst
hace 3 meses
Are you passionate about clinical trials? Do you have experience ensuring compliance with Mexican importation and exportation laws? We are looking for a Clinical Trials Assistant to join our team in Mexico. If that sounds like you, read on and apply today for a life-changing career.
The Position
As a Clinical Trials Senior Analyst at Novo Nordisk, you will:
Be the main contact with importers, couriers, and customs agents, ensuring compliance with importation and exportation laws. Maintain close communication with CDC TMs to align lead time expectations for new trials and ensure availability of medicine and clinical supplies throughout trial development. Anticipate potential risks and take time & effective actions to avoid them, escalating any quality issues to the line manager. Request in advance all necessary information from the importer to ensure that products will be released from customs on time. Follow up on any medicine and clinical supplies to be imported until its final destination, such as Local Depot, Sites, or NN offices. Safeguard company resources by ensuring the best use of them and searching for new ways or providers that make the process more agile without compromising ethics and quality.Qualifications
If you can nod your head at the following attributes, then you could be the person we are looking for:
Degree in Chemist Pharmacobiologist, Pharmaceutical Engineering, Biologist, or a similar field related to health science. At least 3 years of experience as a Clinical Trials Assistant preferable working with Imports with demonstrated skills in core competencies. Knowledge of clinical trials imports and Mexican importation regulations. 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.
