CRA

Novo Nordisk A/S; Buenos Aires; Hybride; ARS 1 200 000 - 1 800 000; Plein temps

Résumé du poste

Novo Nordisk A/S in Argentina seeks a Clinical Research Associate to support execution of clinical trials across the country. You will connect Novo Nordisk with trial sites, ensure studies meet global standards and patient safety remains the top priority.

Responsibilities include monitoring sites, initiating and close-out visits, data verification, and maintaining eTMF/IVRS records, with travel within Argentina about twice per month.

Qualifications

• University degree in Medicine, Pharmacy, Biotechnology or related health sciences.
• 1-2 years of proven experience as a CRA monitoring clinical trials.
• Intermediate to advanced English proficiency (written and spoken).
• Knowledge of ICH-GCP guidelines, Argentine regulatory framework, and eTMF/IVRS.
• Willingness to travel within Argentina approximately twice per month.
• Strong attention to detail and organizational skills; ability to manage multiple sites.
• Excellent interpersonal and communication skills.

Responsabilités

• Monitor trial sites across Argentina for ICH-GCP and study protocol compliance.
• Conduct site initiation, routine monitoring, and close-out visits.
• Review and verify source documents for data quality and regulatory submissions.
• Build relationships with investigators and site staff to support trial execution.
• Manage eTMF documentation and IVRS data entry.
• Identify and resolve site-level issues, escalating when needed.
• Travel within Argentina about twice per month.

Connaissances

CRA monitoring

English proficiency

Attention to detail

Communication skills

Formation

University degree in Medicine, Pharmacy, Biotechnology or related health sciences

Outils

eTMF

IVRS

ICH-GCP knowledge

Description du poste

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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

• 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.

Deadline

Applications are reviewed on an ongoing basis.

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.