Clinical Trials Senior Analyst

hace 2 días


Ciudad de México, Ciudad de México Novo Nordisk A tiempo completo
Clinical Trials Senior Analyst Role

We are seeking a highly skilled Clinical Trials Senior Analyst to join our team in Mexico. As a key member of our clinical development team, you will be responsible for ensuring compliance with importation and exportation laws, maintaining close communication with CDC TMs, and anticipating potential risks to avoid them.

Key Responsibilities
  • Be the main contact with importers, couriers, and customs agents to ensure 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.
  • Anticipate potential risks and take effective actions to avoid them, escalating any quality issues to the line manager.
  • Request necessary information from importers in advance to ensure timely release of products from customs.
  • Follow up on medicine and clinical supplies until their final destination.
  • 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.
Requirements
  • 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, preferably 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 initial planning to 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.

Working at Novo Nordisk

We drive change and strive for excellence without fixating on perfection. We never shy away from opportunities to develop and seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort.



  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    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. If that sounds like you, read on to learn more about this exciting opportunity.The PositionAs a Clinical Trials Senior Analyst, you will be responsible for...


  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    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 in Mexico.The PositionAs a Clinical Trials Senior Analyst, you will be responsible for:Ensuring compliance with importation and exportation laws, maintaining close...


  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    Are you passionate about clinical trials and ensuring compliance with regulations? We are seeking a skilled Clinical Trials Senior Analyst to join our team at Novo Nordisk A/S in Mexico.The PositionAs a Clinical Trials Senior Analyst, you will be responsible for:Coordinating with importers, couriers, and customs agents to ensure compliance with importation...


  • Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

    Are you passionate about clinical trials and ensuring compliance with regulations? We are seeking a skilled Clinical Trials Senior Analyst to join our team at Novo Nordisk A/S in Mexico.The RoleAs a Clinical Trials Senior Analyst, you will be responsible for:Coordinating with importers, couriers, and customs agents to ensure compliance with importation and...


  • Ciudad de México, Ciudad de México Novo Nordisk A tiempo completo

    About the RoleWe are seeking a highly skilled Clinical Trials Senior Analyst to join our team in Mexico. As a key member of our clinical development team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesDevelop and maintain strong relationships with importers, couriers, and customs agents to ensure...


  • Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

    Job OverviewAs a key member of our team, you will be responsible for ensuring the smooth start-up and maintenance of clinical trials in assigned countries. This includes coordinating with investigative sites, collecting and organizing required documents, and interacting with regulatory authorities to ensure compliance with applicable regulations and...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    **About the Role**Worldwide Clinical Trials is seeking a highly organized and detail-oriented Clinical Operations Specialist to join our team. As a Clinical Operations Specialist, you will be responsible for carrying out daily aspects of operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition,...


  • Ciudad de México, Ciudad de México 520 ICR Mexico - MEX A tiempo completo

    Job Title: Senior Regulatory Affairs Specialist with Experience in Clinical TrialsJob Summary:We are seeking a Senior Regulatory Affairs Specialist to join our team at 520 ICR Mexico - MEX. As a Senior Regulatory Affairs Specialist, you will play a key role in ensuring regulatory compliance and facilitating the successful execution of clinical trials.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical trials team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    {"title": "Clinical Trials Project Manager", "content": "Job OverviewAs a Clinical Trials Project Manager at IQVIA, you will lead and oversee the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies.Key Responsibilities:Provide...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    {"Job Overview": "As a Sr. Clinical Trials Assistant at IQVIA, you will play a key role in leading and overseeing the execution of clinical projects and research studies. Your expertise will ensure compliance with global and local regulations, meeting quality and timeline metrics, and providing project-related support to project management...


  • Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

    Job OverviewAs a leading global contract research organization (CRO), Fortrea is seeking a highly motivated and detail-oriented Clinical Trials Specialist to join our team. In this role, you will be responsible for coordinating and collecting data and information required by regulatory authorities, including the preparation of study documentation and...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Trials Project Manager to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key ResponsibilitiesProvide project-related support to...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    **About the Role**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Worldwide Clinical Trials. As a key member of our team, you will be responsible for planning, initiating, and tracking documents required for regulatory submissions, essential documents collection, review, and provision of country/site/EC requirements to...


  • Ciudad de México, Ciudad de México Novo Nordisk A tiempo completo

    Position OverviewWe are seeking a highly skilled and experienced Clinical Trials Coordinator to join our team at Novo Nordisk. As a key member of our Clinical Data Science and Evidence team, you will play a pivotal role in managing clinical and real-world evidence studies.Key ResponsibilitiesOversee the lifecycle management of clinical and real-world...