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Clinical Research Associate in Sao Paulo
Novo Nordisk AS
Clinical Research Associate - Banco De Talentos
Ich-gcp guidelinesClinical trial monitoringRisk-based quality managementAs 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
São Paulo, BRJob Match ScoreCreate Profile
12 days agoNovo Nordisk AS
Clinical Research Associate - Banco De Talentos
Ensure qualityProtect patient safetyDrive studies forwardYou'll be at the heart of clinical trials that could change millions of lives
São Paulo, SP, BrazilJob Match ScoreCreate Profile13 days agoAstraZeneca
Monitor De Pesquisa Clínica Oncologia
Advanced english proficiency requiredRobust clinical research monitoring experienceOncology therapeutic area expertise preferredThe role involves conducting remote and on-site visits including selection, initiation, interim monitoring, and study closure for oncology clinical trials
São Paulo, BrazilNot specifiedFull timeExperience requiredJob Match ScoreCreate Profile17 days agoAstraZeneca
Monitor De Pesquisa Clínica Oncologia
Oncology clinical research experienceIch-gcp guidelines knowledgeRemote and onsite monitoring visitsThis role offers the opportunity to work at the forefront of oncology science to transform cancer treatment practices
São Paulo, BrazilNot specified (assumed to include travel)Full timeExperience requiredJob Match ScoreCreate Profile17 days agoJohnson & Johnson
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceGood clinical practice (gcp) complianceSite initiation and close-out activitiesThis 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
São Paulo, BrazilFull time+5y experienceJob Match ScoreCreate Profile18 days agoAstraZeneca
Monitor De Pesquisa Clínica Oncologia
Oncology clinical research experienceIch-gcp guidelines knowledgeRemote and on-site monitoring visitsThis role offers the opportunity to work at the forefront of oncology science, contributing to studies that can transform medical practice
São Paulo, BrazilFull timeExperience requiredJob Match ScoreCreate Profile19 days agoBeOne
Regional Clinical Trial Management Associate
Fluent english language proficiency2+ years clinical trials experienceSite level cro or pharmacy industry backgroundThe role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile20 days agobeonemedicines.sg
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trials experienceKnowledge of ich guidelines and regulationsThe role supports the Regional Clinical Study Manager in delivering regional studies while ensuring execution meets quality standards, timelines, and budget
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile21 days agoJohnson & Johnson
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceBachelor's degree in pharmacy or life sciencesProficient knowledge of gcp and local regulationsThis role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance
São Paulo, BrazilFull time+5y experienceJob Match ScoreCreate Profile21 days agoJohnson & Johnson MedTech
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceBachelor's degree in pharmacy or life sciencesProficiency in gcp, sops, and local regulationsThis role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance
São Paulo, BrazilFull time+5y experienceJob Match ScoreCreate Profile21 days agoJ&J FAMILY OF COMPANIES
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceGood clinical practice (gcp) complianceSite initiation and close-out activitiesThis role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness
São Paulo, BrazilFull time+5y experienceJob Match ScoreCreate Profile21 days agoBeiGene
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trial experienceSite level or cro backgroundThe role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile22 days agobeonemedicines.us
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trial experienceKnowledge of ich guidelines and regulationsThe role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
São Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile22 days agoBeOne Medicines
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trial experienceSite level and cro operations knowledgeThe role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile22 days agobeonemedicines.ar
Regional Clinical Trial Management Associate
Fluent english language proficiency2+ years clinical trials experienceKnowledge of ich guidelines and regulationsThis role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring adherence to quality standards, timelines, and budgets
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile22 days agoBeOne
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trials experienceSite level and cro operations knowledgeThe role supports the Regional Clinical Study Manager in delivering regional study components while ensuring execution meets quality standards, timelines, and budget
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile22 days agoBeOne
Regional Clinical Trial Management Associate
Fluent english language proficiency2+ years clinical trials experienceKnowledge of ctms and etmf systemsThe role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget
Sao Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile23 days agoJohnson & Johnson
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceGood clinical practice (gcp) complianceSite initiation and close-out activitiesThis 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
São Paulo, BrazilFully remoteFull time+5y experienceJob Match ScoreCreate Profile23 days agobeonemedicines.nl
Regional Clinical Trial Management Associate
Fluent english language skills2+ years clinical trials experienceKnowledge of ich guidelines and regulationsThe role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget
São Paulo, BrazilHybridFull time+2y experienceJob Match ScoreCreate Profile23 days agoJohnson & Johnson UK
Sr. Site Manager (sr. Cra - Monitor De Pesquisa Clínica Sr) - São Paulo
3-5 years clinical trial monitoring experienceGood clinical practice (gcp) complianceSite initiation and close-out activitiesThis role serves as the primary contact point between the Sponsor and Investigational Site to ensure inspection readiness through strict compliance with protocols and regulations
São Paulo, BrazilFully remoteFull time+5y experienceJob Match ScoreCreate Profile23 days agoAbbVie
Clinical Research Associate Ii
On-site monitoring of investigational drug trialsKnowledge of ich/gcp guidelines and regulationsExperience with protocol execution and close-outThe role involves proactively solving study-related clinical site issues to ensure successful protocol level execution across start-up, execution, and close-out phases
São Paulo, BrazilOn-siteFull time+1y experienceJob Match ScoreCreate Profile24 days agoICON plc
Graduate Pharmacovigilance Associate
Bachelor's degree in pharmacy or life sciencesStrong attention to detail and organizational skillsProficiency in microsoft office applicationsCompetitive salary mentioned
ICON plc is seeking a Graduate Pharmacovigilance Associate to support the safety monitoring and reporting of pharmaceutical products
Full timeJuniorJob Match ScoreCreate Profile29 days agoICON plc
Clinical Research Associate I
University degree in medicine or scienceKnowledge of ich-gcp guidelinesAbility to travel at least 60% of timeCompetitive salary mentioned
ICON plc is a world-leading healthcare intelligence organization seeking a Clinical Research Associate to join their diverse team in São Paulo
São Paulo, BrazilFull timeExperience requiredJob Match ScoreCreate Profile29 days agoBeOne
Study Start-up Head, Latam
8+ years clinical research experience6+ years study start-up in latin americaFluent english language proficiencyThe role involves leading the identification, selection, activation, and maintenance of clinical sites for complex oncology trials across the LATAM region
Sao Paulo, BrazilHybridFull time+8y experienceJob Match ScoreCreate Profile29 days agoIQVIA Inc
Cra 2 - Brazil
Good clinical practice gcp complianceInternational conference harmonization ich guidelinesSite monitoring visits executionCompetitive salary + benefits pyckage
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements
Sao Paulo, BrazilFull timeJob Match ScoreCreate Profile30 days ago
