Clinical Trials Senior Analyst (Imports)

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.

Working at Novo Nordisk

At Novo Nordisk, we don’t wait for change. We drive change. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 64,000 employees to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further.

Contact

To complete your application, please click in "Apply now" attach your CV and follow de instructions. For more information, please follow us on LinkedIn: Novo Nordisk: About | LinkedIn

Deadline

Apply before October 20th, 2024.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in.

Together, we’re life changing.