CRA Jr.

About the Department

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We’re changing lives for a living. Are you ready to make a difference?

Job description

Location

Buenos Aires (Vicente López), Argentina – field-based, with site visits across Buenos Aires and other provinces

Job category

Clinical Development

Job title: Clinical Research Associate Junior

Department: Clinical Operations, Novo Nordisk Argentina

Location: Buenos Aires (Vicente López), Argentina. Field-based role with regular visits to research sites in Buenos Aires and other provinces, working remotely when not on site.

Your impact begins here

As a Clinical Research Associate, you will make sure clinical trials at sites across Argentina run safely, on time and to a high standard. You will be the main link between Novo Nordisk, investigators and site teams, protecting data quality and the safety and rights of the people taking part. As our Clinical Operations team grows, you will help deliver trials in diabetes, obesity, cardiovascular and metabolic disease – research that shapes future treatment for people living with these conditions.

What you’ll bring

You are at an early stage of your clinical research career and ready for your next step. You will bring:

• A degree in health sciences, such as medicine, nutrition, pharmacy, psychology, biochemistry or a related field.
• Early experience in clinical research – ideally from a few months to around one year – for example as a junior CRA, Clinical Trial Administrator (CTA) or in a clinical research support role, including at a CRO.
• Intermediate English, so you can read study documentation, take part in global meetings and communicate confidently in writing.
• Availability to travel regularly to research sites in Buenos Aires and other provinces.
• A proactive, curious and adaptable approach, with the agility to work well in a dynamic environment and openness to change.
• A strong team player mindset and the motivation to keep learning and developing.
• Attention to detail, good organisational skills and a genuine focus on quality and patient safety.
  
  

Essential:

• A clinical monitoring course.
• Certification in or working knowledge of ICH Good Clinical Practice (GCP).
• Experience with a CRO, such as IQVIA, ICON, Syneos or similar.
  
  Useful
• Curiosity about artificial intelligence (AI) and how new digital tools can improve the way trials are run.

What you’ll do

You will manage around eight trial sites, giving them the support they need to deliver high-quality studies. Your work will include:

• Conducting on-site and remote monitoring visits in line with the protocol, monitoring plan, ICH-GCP, internal procedures and local regulations.
• Protecting patient safety and data integrity by reviewing site data, resolving discrepancies and making sure adverse events are handled correctly.
• Following site performance, recruitment, retention and data collection, and acting early on issues that could affect timelines or quality.
• Applying risk-based quality management to identify, assess and reduce risks throughout the study, and keeping sites inspection-ready.
• Training and supporting site staff on protocols, systems and procedures, and managing investigational product, study supplies and essential documents, including the Investigator Trial Master File.
• Building strong relationships with investigators and site teams, and sharing site insights that help improve protocols, patient engagement and ways of working.

Who you’ll work with

You will join Clinical Operations in Argentina, a team of around 60 people, including roughly 35 monitors and seven managers. You will report to a Clinical Operations manager, who will support you closely as you build your experience.

Outside Novo Nordisk, your closest partners will be investigators, study nurses and coordinators at research sites. You may also work with ethics committees, local health authorities and vendors. Inside Novo Nordisk, you will collaborate with Trial Managers, the Study Start-up team, Vendor Managers and global trial teams, taking part in investigator meetings, CRA training and trial meetings. Together, you will keep studies moving with clarity and pace, and make sure what you learn at site level shapes decisions across the trial.

What you can expect here

Working on the sponsor side, you will see how clinical trials are designed, run and improved – and contribute to studies that matter for people living with serious chronic diseases. You will grow on the job with close guidance from your manager, and there are opportunities to progress your career, including promotion and moves into other roles as you develop.

You will join an established, collaborative team where people support each other, speak up and are trusted to take ownership of their sites. Our field-based model, with remote work between site visits, is designed to give you flexibility in how you organise your week.

Start now

Your impact begins today. If you are ready to help bring high-quality clinical research to people across Argentina, apply for the Clinical Research Associate role by 8 October 2026. We are hiring for several positions and reviewing applications on an ongoing basis, so we encourage you to apply as soon as possible.

If you have been referred by a Novo Nordisk colleague, please apply through this advert.

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

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.