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Brazil Browse · Sao Paulo · Clinical Research Associate

Clinical Research Associate in Sao Paulo

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Monitor De Pesquisa Clínica Oncologia
AstraZeneca
São Paulo, Brazil
Full time
Not specified
Advanced english proficiency required
Robust clinical research monitoring experience
Oncology therapeutic area expertise preferred
The role involves conducting remote and on-site visits including selection, initiation, interim monitoring, and study closure for oncology clinical trials
3 days ago
Monitor De Pesquisa Clínica Oncologia
AstraZeneca
São Paulo, Brazil
Full time
Not specified (assumed to include travel)
Oncology clinical research experience
Ich-gcp guidelines knowledge
Remote and onsite monitoring visits
This role offers the opportunity to work at the forefront of oncology science to transform cancer treatment practices
3 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
Johnson & Johnson
São Paulo, Brazil
Full time
**
3-5 years clinical trial monitoring experience
Good clinical practice (gcp) compliance
Site initiation and close-out activities
This role serves as the primary contact point between the Sponsor and Investigational Site to ensure inspection readiness through strict compliance with GCP and company SOPs
4 days ago
Monitor De Pesquisa Clínica Oncologia
AstraZeneca
São Paulo, Brazil
Full time
**
Oncology clinical research experience
Ich-gcp guidelines knowledge
Remote and on-site monitoring visits
This role offers the opportunity to work at the forefront of oncology science, contributing to studies that can transform medical practice
5 days ago
Regional Clinical Trial Management Associate
BeOne
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language proficiency
2+ years clinical trials experience
Site level cro or pharmacy industry background
The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
6 days ago
Regional Clinical Trial Management Associate
beonemedicines.sg
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trials experience
Knowledge of ich guidelines and regulations
The role supports the Regional Clinical Study Manager in delivering regional studies while ensuring execution meets quality standards, timelines, and budget
6 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
Johnson & Johnson
São Paulo, Brazil
Full time
**
3-5 years clinical trial monitoring experience
Bachelor's degree in pharmacy or life sciences
Proficient knowledge of gcp and local regulations
This role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance
7 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
Johnson & Johnson MedTech
São Paulo, Brazil
Full time
**
3-5 years clinical trial monitoring experience
Bachelor's degree in pharmacy or life sciences
Proficiency in gcp, sops, and local regulations
This role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance
7 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
J&J FAMILY OF COMPANIES
São Paulo, Brazil
Full time
**
3-5 years clinical trial monitoring experience
Good clinical practice (gcp) compliance
Site initiation and close-out activities
This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness
7 days ago
Regional Clinical Trial Management Associate
BeiGene
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trial experience
Site level or cro background
The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
8 days ago
Regional Clinical Trial Management Associate
beonemedicines.us
São Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trial experience
Knowledge of ich guidelines and regulations
The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
8 days ago
Regional Clinical Trial Management Associate
BeOne Medicines
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trial experience
Site level and cro operations knowledge
The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
8 days ago
Regional Clinical Trial Management Associate
beonemedicines.ar
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language proficiency
2+ years clinical trials experience
Knowledge of ich guidelines and regulations
This role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring adherence to quality standards, timelines, and budgets
8 days ago
Regional Clinical Trial Management Associate
BeOne
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trials experience
Site level and cro operations knowledge
The role supports the Regional Clinical Study Manager in delivering regional study components while ensuring execution meets quality standards, timelines, and budget
8 days ago
Regional Clinical Trial Management Associate
BeOne
Sao Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language proficiency
2+ years clinical trials experience
Knowledge of ctms and etmf systems
The role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget
9 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
Johnson & Johnson
São Paulo, Brazil
Full time
Fully remote
3-5 years clinical trial monitoring experience
Good clinical practice (gcp) compliance
Site initiation and close-out activities
This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness through strict compliance with protocols and regulations
9 days ago
Regional Clinical Trial Management Associate
beonemedicines.nl
São Paulo, Brazil
Full time
Hybrid
+2y experience
Fluent english language skills
2+ years clinical trials experience
Knowledge of ich guidelines and regulations
The role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget
9 days ago
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
Johnson & Johnson UK
São Paulo, Brazil
Full time
Fully remote
3-5 years clinical trial monitoring experience
Good clinical practice (gcp) compliance
Site initiation and close-out activities
This role serves as the primary contact point between the Sponsor and Investigational Site to ensure inspection readiness through strict compliance with protocols and regulations
9 days ago
Clinical Research Associate Ii
AbbVie
São Paulo, Brazil
Full time
On-site
+1y experience
On-site monitoring of investigational drug trials
Knowledge of ich/gcp guidelines and regulations
Experience with protocol execution and close-out
The role involves proactively solving study-related clinical site issues to ensure successful protocol level execution across start-up, execution, and close-out phases
10 days ago
Graduate Pharmacovigilance Associate
ICON plc
Full time
Not specified; competitive salary mentioned; vario...
Junior
Bachelor's degree in pharmacy or life sciences
Strong attention to detail and organizational skills
Proficiency in microsoft office applications
ICON plc is seeking a Graduate Pharmacovigilance Associate to support the safety monitoring and reporting of pharmaceutical products
15 days ago
Clinical Research Associate I
ICON plc
São Paulo, Brazil
Full time
Not specified; competitive salary mentioned; vario...
University degree in medicine or science
Knowledge of ich-gcp guidelines
Ability to travel at least 60% of time
ICON plc is a world-leading healthcare intelligence organization seeking a Clinical Research Associate to join their diverse team in São Paulo
15 days ago
Study Start-up Head, Latam
BeOne
Sao Paulo, Brazil
Full time
Hybrid
+8y experience
8+ years clinical research experience
6+ years study start-up in latin america
Fluent english language proficiency
The role involves leading the identification, selection, activation, and maintenance of clinical sites for complex oncology trials across the LATAM region
15 days ago
Cra 2 - Brazil
IQVIA Inc
Sao Paulo, Brazil
Full time
Not specified; not specified; competitive salary +...
Good clinical practice gcp compliance
International conference harmonization ich guidelines
Site monitoring visits execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements
16 days ago
Cra 2 - Brazil
IQVIA UK
Sao Paulo, Brazil
Full time
Not specified; not specified; competitive salary +...
Good clinical practice (gcp) knowledge
Ich guidelines application
Site monitoring visit execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines
16 days ago
Cra 1 - Brazil
IQVIA Inc
Sao Paulo, Brazil
Full time
Not specified; not specified; competitive salary +...
Good clinical practice gcp knowledge
Ich guidelines application
Site monitoring visit execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements
16 days ago

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Clinical Research Associate in Sao Paulo

Monitor De Pesquisa Clínica Oncologia

Monitor De Pesquisa Clínica Oncologia

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Monitor De Pesquisa Clínica Oncologia

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Regional Clinical Trial Management Associate

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Regional Clinical Trial Management Associate

Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo

Clinical Research Associate Ii

Graduate Pharmacovigilance Associate

Clinical Research Associate I

Study Start-up Head, Latam

Cra 2 - Brazil

Cra 2 - Brazil

Cra 1 - Brazil