CRA

Novo Nordisk A/S; Partido de Vicente López; Presencial; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

Novo Nordisk A/S in Argentina is seeking a Clinical Research Associate to ensure trials meet global standards and patient safety across sites. You will monitor sites, initiate visits, verify data, manage eTMF and IVRS, and build strong PI relationships to support study execution.

The role requires a university health sciences degree, 1-2 years CRA experience, and good English. Travel across Argentina about twice per month.

Formación

• University degree in Medicine, Pharmacy, Biotechnology, QFB or related health sciences.
• 1-2 years of proven CRA monitoring experience.
• Intermediate to advanced English proficiency.
• Solid knowledge of ICH-GCP guidelines and Argentine regulatory framework.
• Ability to travel within Argentina approximately twice per month.

Responsabilidades

• Monitor clinical trial sites to ensure compliance with ICH-GCP and study protocols.
• Conduct site initiation, routine monitoring, and close-out visits.
• Review source documents and ensure data quality for regulatory submissions.
• Build strong relationships with principal investigators and site staff.
• Manage eTMF documentation and IVRS systems for accurate data entry.
• Identify and resolve site-level issues, escalating when needed.

Conocimientos

Clinical Research

English Proficiency

Educación

Medicine degree

Pharmacy degree

Biotechnology/Health sciences degree

Herramientas

eTMF

IVRS

Descripción del empleo

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As a Clinical Research Associate, you'll play a critical role in the successful execution of clinical trials across Argentina. You'll be the vital link between Novo Nordisk and clinical trial sites, ensuring that our studies are conducted with integrity, in compliance with global standards, and with patient safety as the top priority.

Your responsibilities will include:

Monitoring clinical trial sites across Argentina to ensure compliance with ICH-GCP guidelines, study protocols, and regulatory requirements

Conducting site initiation, routine monitoring, and close-out visits at investigator sites

Reviewing and verifying source documents, ensuring data quality and integrity for submission to regulatory authorities

Building strong relationships with principal investigators, study coordinators, and site staff to support successful trial execution

Managing eTMF documentation and IVRS systems, ensuring accurate and timely data entry

Identifying and resolving site-level issues proactively, escalating when necessary

Traveling within Argentina approximately twice per month to visit clinical trial sites

Your new department

Within International Operations, Clinical Trials Operations is responsible for the operational execution of clinical studies that bring innovative treatments to patients. Our team works across diverse therapy areas, collaborating with investigators, healthcare professionals, and cross-functional partners to ensure every trial meets rigorous quality standards. Your work will directly contribute to expanding access to breakthrough medicines for patients living with serious chronic diseases.

Your skills & qualifications

We're looking for an experienced Clinical Research Associate who is passionate about clinical research and committed to patient safety. You'll bring with you:

University degree in Medicine, Pharmacy, Biotechnology, QFB (Chemical Pharmaceutical Biology) or related health sciences

1- 2 years of proven experience as a CRA monitoring clinical trials

Intermediate to advanced English proficiency (written and spoken)

Solid working knowledge of ICH-GCP guidelines, Argentine regulatory framework, and clinical trial platforms including eTMF and IVRS

Availability to travel within Argentina approximately twice per month

Strong attention to detail, organizational skills, and ability to manage multiple sites simultaneously

Excellent interpersonal and communication skills to build effective relationships with site personnel

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

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

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

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