CRA - CLINICAL RESEARCH ASSOCIATE (TALENT PIPELINE)

Step into the Future.
Join Novo Nordisk's Talent Pipeline! Are you ready to shape the future of healthcare with Novo Nordisk? We are thrilled to announce an opportunity within our Talent Pipeline, where we actively seek top-tier professionals to join our pioneering team in the first semester of.
The Talent Pipeline provides an exceptional opportunity for you to submit your application and initiate a meaningful dialogue with us.
Ready to advance your career in Clinical Research? Join us as a Clinical Research Associate (CRA) and play a crucial role in ensuring the meticulous execution and documentation of clinical studies, strictly adhering to protocols, guidelines, regulations, and effective standard operating procedures.
Become a part of pioneering research and apply today! The Position As a CRA - Clinical Research Associate you will be responsible for ensuring that our research is monitored and that it meets the expected standards, always keeping up to date with local and international rules and regulations related to clinical research and corporate standards, always acting within the expected quality standards.
Your responsibilities will also include.
Drafting, reviewing and maintaining essential documents relating to NN projects, providing support.
Supporting the preparation and control of budgets and payments, as well as contracts with centres, investigators, suppliers and service providers.
Assisting the Clinical Research Coordinator in clinical study management activities Requesting, controlling and sending medication and clinical study materials to the respective centres as required by the study.
Planning and carrying out external visits to the study sites for selection, project initiation, site monitoring and study closure, as well as updating the clinical research monitoring systems with all the data collected during the visits.
Qualifications You have a University Degree in the health area; It is expected knowledge of monitoring clinical research as a Clinical Research Associate; You have an advanced level of English in reading, writing and speaking, as well as fluent or native Portuguese; 40% of travel availability; It will be a plus if you have experience with Clinical Trial Management Systems, remote monitoring and working with complex projects as oncology and cardiology for example.
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