Clinical Research Associate - Banco de Talentos

Novo Nordisk; São Paulo; In loco; BRL 180.000 - 260.000; Tempo pieno

Descrizione del lavoro

Novo Nordisk in São Paulo seeks a Clinical Research Associate to serve as the primary liaison between Novo Nordisk and clinical trial sites, ensuring study execution adheres to protocol and safety standards.

In this role, you will monitor sites, manage data quality, and support cross-functional teams to drive patient safety and study progress in Novo Nordisk's innovative pipeline.

Competenze

• Bachelor's degree in Life Sciences or related field.
• Experience in clinical trial monitoring or a relevant pharma/CRO role.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Excellent written and verbal communication skills.
• Strong organizational and time management skills.
• Proficiency with EDC, CTMS, and eTMF tools.
• Proactive risk identification and mitigation.
• Willingness to travel as required.

Mansioni

• Conducting on-site and remote monitoring visits per ICH-GCP and regulations.
• Managing clinical trial sites as main contact, overseeing performance and data collection.
• Implementing RBQM principles to identify and mitigate risks.
• Building relationships with investigators, site staff, and cross-functional teams.
• Ensuring patient safety and data integrity by monitoring adverse events and queries.
• Leading site training and supporting study protocols and digital systems.
• Managing IMP, study supplies, and essential documents across sites.

Formazione

Bachelor's degree in Life Sciences

Strumenti

EDC systems

CTMS

eTMF

Descrizione del lavoro

Clinical Research Associate

Ready to be the link between groundbreaking science and the patients who need it most? As a Clinical Research Associate at Novo Nordisk, you'll be at the heart of clinical trials that could change millions of lives—ensuring quality, protecting patient safety, and driving studies forward from protocol to completion.

This opportunity is part of a talent pool designed to support the expected hiring demand between June and September 2026, offering the chance to be considered for upcoming openings within this period.

Your new role

As a Clinical Research Associate, you'll serve as the primary liaison between Novo Nordisk and clinical trial sites, taking ownership of study execution while building meaningful relationships with investigators and site staff. You'll be trusted to ensure compliance, quality, and patient safety across every aspect of your assigned studies.

Your key responsibilities will include:

• Conducting on-site and remote monitoring visits in accordance with ICH-GCP guidelines, regulatory requirements, and internal protocols to ensure the highest standards of trial execution
• Managing clinical trial sites as the main point of contact, overseeing site performance, recruitment progress, data collection, and resolution of discrepancies
• Implementing risk-based quality management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct
• Building and maintaining strong relationships with investigators, site staff, and cross-functional teams to support smooth study execution and the Novo Nordisk drug pipeline
• Ensuring patient safety and data integrity by monitoring adverse events, resolving data queries, and maintaining compliance with protocols and regulatory standards
• Leading site training and providing continuous support on study protocols, operational procedures, and digital systems
• Managing investigational medicinal products (IMP), study supplies, essential documents, and equipment across sites to ensure accountability and quality

Your new department

In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

Within R&D, you'll join the Clinical Trials team – a dynamic group dedicated to bringing new treatments from concept to patients. As a CRA, you'll work across multiple therapeutic areas, collaborating with trial managers, study start‑up teams, vendor managers, and site staff to ensure clinical studies are executed with the highest quality standards. Your work directly impacts our ability to develop life‑changing medicines for people living with serious chronic diseases.

Your skills & qualifications

We're looking for someone who thrives in dynamic environments and is passionate about clinical research quality and patient safety. To succeed in this role, you'll need:

• A Bachelor's degree in Life Sciences or a related field
• Experience in clinical trial monitoring or a relevant pharmaceutical industry/CRO role
• Strong understanding and knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial methodology
• Excellent written and verbal communication skills with the ability to build and maintain relationships across all organizational levels
• Strong organizational and time management skills, with the ability to manage multiple sites and priorities simultaneously
• Proficiency in digital tools, including electronic data capture (EDC) systems, CTMS, eTMF, and other clinical trial software
• Problem‑solving capabilities with a proactive approach to risk identification and mitigation
• Flexibility to travel as required to support clinical trial sites

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 andthe 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.

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.