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Clinical Research Associate in Paris
IQVIA Holdings
Experienced Clinical Research Associate, Multi-sponsor, France
2 years clinical oncology experienceBachelor's degree in scientific disciplineProficiency in microsoft office suiteThe role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice standards
Paris, FranceHybridFull time+2y experienceJob Match ScoreCreate Profile
18 days agomicrosatsystems.biz
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe role involves supporting clinical monitoring activities at headquarters and on-site across France for international programs
La Défense, FranceFull timeJob Match ScoreCreate Profile21 days agoIQVIA Holdings
Clinical Research Associate - Iqvia Biotech (homebased In Paris)
Good clinical practice (gcp) knowledgeIch guidelines applicationSite monitoring visit executionThe role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies
Paris, FranceFull time+1y experienceJob Match ScoreCreate Profile22 days agoMerck & Co., Inc.
Alternance Attaché(e) De Recherche Clinique H/f
Clinical trial monitoring experienceRegulatory framework knowledgeStrong organizational skillsThe role involves supporting clinical trial activities from site selection to study closure across France
La Défense, FranceFull timeExperience requiredJob Match ScoreCreate Profile23 days agoSyneosHealth
Experimented Cra In Oncology - Single Sponsor - Based In Paris Area (home Based)
Oncology therapeutic area experienceGood clinical practice (gcp) knowledgeClinical trial monitoring expertiseThe role involves conducting on-site and remote monitoring of clinical research studies in the oncology sector to ensure regulatory compliance
Paris, FranceFully remoteFull time+4y experienceJob Match ScoreCreate Profile24 days agoMerck & Co., Inc.
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe role involves supporting clinical monitoring activities at headquarters and across sites throughout France
La Défense, FranceFull timeJob Match ScoreCreate Profile24 days agoMerck & Co., Inc.
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in written and spoken englishThe role involves supporting clinical program execution, site selection, and study closure activities across France
La Défense, FranceFull timeJob Match ScoreCreate Profile26 days agoMerck & Co., Inc.
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe role offers a 360-degree view of clinical research departments through close collaboration with Clinical Research Associates, Project Managers, and Regulatory teams
La Défense, FranceFull timeJob Match ScoreCreate Profile26 days agoMerck & Co., Inc.
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe intern will support clinical monitoring activities from site selection to study closure across France
La Défense, FranceFull timeJob Match ScoreCreate Profile27 days agoleHACK
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe role offers an opportunity to support clinical trial monitoring activities both at headquarters and on-site across France
La Défense, FranceFull timeJob Match ScoreCreate Profile27 days agoSanofi
Alternance 12 Mois – Technicien.ne D’études In Vivo
Bachelor's degree in life sciencesIntermediate english proficiencyExcel mastery requiredAttractive remuneration
You will participate in the digitization of animal tracking and conduct in vivo pharmacokinetic studies
Vitry-sur-Seine, FranceFull timeExperience requiredJob Match ScoreCreate Profile28 days agoMy Medical Sales Jobs
Experienced Clinical Research Associate, Multi-sponsor, France
2 years clinical oncology experienceGood clinical practice (gcp) knowledgeSite monitoring visit executionThe role requires conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice guidelines
Paris, FranceHybridFull time+2y experienceJob Match ScoreCreate Profile29 days agomedhunter.de
Alternance Attaché(e) De Recherche Clinique H/f
Knowledge of clinical trial regulatory frameworkStrong time management and organizational skillsFluency in english written and oral communicationThe role offers a 360-degree view of clinical research departments including collaboration with project managers and regulatory teams
La Défense, FranceFull timeJob Match ScoreCreate Profile29 days agomed-in.at
Alternance Attaché(e) De Recherche Clinique H/f
Clinical trial monitoring supportRegulatory framework knowledgeTime management and organizationThe role offers a 360-degree view of clinical research careers with close collaboration across Clinical Research, Project Management, Operations, and Regulatory teams
La Défense, FranceFull timeJob Match ScoreCreate Profile29 days agoIQVIA Biotech
Clinical Research Associate - Iqvia Biotech (homebased In Paris)
Perform site monitoring visitsAdhere to gcp and ich guidelinesManage subject recruitment plansThe role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies
Paris, FranceFull time+1y experienceJob Match ScoreCreate Profile29 days agoIQVIA
Experienced Clinical Research Associate, Multi-sponsor, France
2 years clinical oncology experienceGood clinical practice (gcp) knowledgeSite monitoring visit executionThe role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice guidelines
Paris, FranceHybridFull time+2y experienceJob Match ScoreCreate Profile29 days agoSyneosHealth
Senior Cra Ii In Oncology - Sponsor Dedicated - Home Based Paris Area
Oncology therapeutic area expertiseIch-gcp and gpp regulatory knowledgeSite qualification and initiation visitsThe role involves performing comprehensive site management activities including qualification, initiation, interim monitoring, and close-out visits for oncology studies
Paris, FranceFully remoteFull timeExperience requiredJob Match ScoreCreate Profile30 days agoSyneos Health
Experimented Cra In Oncology - Single Sponsor - Based In Paris Area (home Based)
Oncology clinical research experienceGood clinical practice gcp knowledgeSite monitoring and complianceThe role involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices
Paris, FranceFully remoteFull time+4y experienceJob Match ScoreCreate Profile30 days agoSyneos Health
Senior Cra Ii In Oncology - Sponsor Dedicated - Home Based Paris Area
Site qualification and initiation visitsIch-gcp and regulatory compliance knowledgeSource document review and data verificationThe role involves performing comprehensive site management activities including qualification, initiation, interim monitoring, and close-out visits for oncology studies
Paris, FranceFully remoteFull timeExperience requiredJob Match ScoreCreate Profile30 days agoIQVIA UK
Clinical Research Associate - Iqvia Biotech (homebased In Paris)
Perform site monitoring visitsAdhere to gcp and ich guidelinesManage subject recruitment plansThe role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies
Paris, FranceFull time+1y experienceJob Match ScoreCreate Profile30 days agoIQVIA UK
Experienced Clinical Research Associate, Multi-sponsor, France
2 years clinical oncology experienceGood clinical practice (gcp) knowledgeInternational conference on harmonization (ich) guidelinesThe role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice standards
Paris, FranceHybridFull time+2y experienceJob Match ScoreCreate Profile30 days agoParexel
Senior Clinical Research Associate (oncology Experience Required) - Paris Region, France (remote) - Fsp
Oncology trial experience requiredRecist criteria knowledge essentialIch gcp compliance expertiseThe Senior CRA is responsible for ensuring data integrity, quality, and compliance with ICH GCP and local requirements at the site level
Paris, FranceFully remoteFull timeExperience requiredJob Match ScoreCreate Profile31 days agoIQVIA Biotech
Clinical Research Associate - Iqvia Biotech (homebased In Paris)
Site monitoring visits (siv, rmv, cov)Good clinical practice (gcp) complianceSubject recruitment plan managementThe role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines
Paris, FranceFull time+1y experienceJob Match ScoreCreate Profile31 days agoMerck Sharp & Dohme Corp
Alternance Attaché(e) De Recherche Clinique H/f
Clinical trial monitoring supportRegulatory framework knowledgeTime management and organizationThe role offers a 360-degree view of clinical research departments through close collaboration with Clinical Research Associates, Project Managers, and Regulatory teams
La Défense, FranceFull timeJob Match ScoreCreate Profile31 days agoLaboratory Animal Management Association
Alternance Attaché(e) De Recherche Clinique H/f
Clinical trial monitoring supportRegulatory framework knowledgeStrong organizational skillsThe role offers a 360-degree view of clinical research departments including close collaboration with project managers and regulatory teams
La Défense, FranceFull timeJob Match ScoreCreate Profile31 days ago
