Novo Nordisk

Clinical Research Associate - Banco de Talentos (São Paulo, São Paulo, BR)

São Paulo, Brazil Type not listed
Clinical Development Associate

Novo Nordisk is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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Clinical Research Associate

São Paulo, SP, Brazil

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 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.

More information  

For more information, visit   novonordisk.com,    Facebook,  Instagram ,   X ,   LinkedIn   and  YouTube.  To complete your application, click on "Apply now", attach your CV and follow the instructions.

Deadline  

Please apply before September 12

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.

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Job details

Seniority
Associate
Function
Clinical Development
Therapeutic area
Not listed
Location
São Paulo, Brazil
Employment type
Not listed

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 194 comparable Associate Clinical Development roles across 37 biopharma companies.

194Comparable roles tracked
179Currently active
37Companies hiring similar roles
29Countries represented

Salary context

47 of 194 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Clinical Trials Data Associate (P1) · Lilly $79,206/yr – $91,087/yr
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $85,146 – $259,448 (median $168,090)

Where these roles are based

Top locations among the 194 comparable roles

United States69
India42
United Kingdom12
China11
Poland8
Germany6

+ 23 more countries

Seniority mix

194 of 194 peers have a known seniority level

Manager146
Associate47
Intern/Fellow/Postdoc1

Therapeutic area mix

16 of 194 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Cardiovascular / CVRM4
Immunology2
Neuroscience1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Biogen Sao Paulo, Brazil Associate
Same function Same seniority Same country
45%similar
AstraZeneca Warsaw, Poland Associate
Same function Same seniority
45%similar
AstraZeneca Hamburg, Germany Associate
Same function Same seniority
45%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority
45%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority
45%similar
AbbVie North Chicago, IL Associate
Same function Same seniority

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Clinical Country and Site Lead
Biogen · Sao Paulo, Brazil · Associate
Function Therapeutic area Seniority Country
45%
GRA Regulatory Delivery Excellence, Clinical Regulatory Associate
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
45%
Clinical Research Associate II
AbbVie · Boston, MA · Associate
Function Therapeutic area Seniority Country
45%
Clinical Research Associate II
AbbVie · Belgrade, rs · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.