11 Clinical Data And Biostatistics jobs in São Paulo.

Hiring now: Site Care Partner Fsp @ Parexel, Clinical Trial Asst @ Iqvia, Medical Monitor @ Psi, Sr Database Dev @ Psi Cro, Sr Site Mgr Sr Clinical R @ Johnson Jo.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (5) Functional Service Provider (3) CRA (3) Site Care Partner (3) Project Leadership (2) Biostatistics (2) Data Management (2) Clinical Research (2) Monitoring (2) data analysis (2)

📍 Locations

São Paulo (11)

Parexel

Skills & Focus: Clinical Trials, Functional Service Provider, CRA, Site Care Partner, Project Leadership, Statistical Programming, Consulting, Finance, Remote, Biostatistics
About the Company: Parexel is a leading global provider of biopharmaceutical services, working closely with clients to advance new therapies to market.
Skills & Focus: Clinical Trials, Functional Service Provider, CRA, Site Care Partner, Project Leadership, Biostatistics, Data Management, Medical Writing, Health Economics, Regulatory Strategy

Iqvia

Skills & Focus: Clinical Trial Assistant, administrative activities, Trial Master File, clinical documents, site compliance, case report forms, effective time management, clinical monitoring, good command of English, documentation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3 years administrative support experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Parexel

Skills & Focus: CRA, Clinical Trials, Functional Service Provider, Site Care Partner, Clinical Research, Monitoring, Data Management, Healthcare, Regulatory Consulting, Biopharmaceutical
About the Company: Parexel is a leading global biopharmaceutical services organization, specializing in clinical research and regulatory consulting.

Iqvia

Skills & Focus: clinical trial management, project delivery, regulatory compliance, clinical quality, stakeholder management, risk mitigation, recruitment targets, data analysis, monitoring, life sciences
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 7 years clinical research/monitoring experience; or equivalent combination of education, training and experience. At least 2-3 years leading clinical research studies (regional and/or globally speaking).
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Psi

Skills & Focus: clinical studies, medical input, patient safety, data analysis, clinical development plans, protocols, safety issues, Pharmacovigilance, mitigation strategies, GCP guidelines
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Parexel

Skills & Focus: Clinical Research Associate, site management, monitoring, patient safety, investigator sites, site activation, recruitment planning, data entry timelines, quality assurance, investigator relationships
About the Company: Parexel is a leading global biopharmaceutical services organization, helping clients accelerate the journey from lab to life.

Psi Cro

Skills & Focus: SAS Developer, clinical database development, database programming, data validation, CDISC-compliant, SDTM, data management, electronic data transfer, clinical trial data, data tracking
About the Company: A global provider of clinical development services, specializing in data management and programming services for clinical trials.

Iqvia

Skills & Focus: Clinical Research, Study Coordinator, Clinical Trials, Nursing, Patient Data, Medical Terminology, Regulatory Documents, Administrative Tasks, Electronic Data Capture, CTMS
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Previous experience as Study Coordinator
Type: Part-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
CRA 2 São Paulo
Skills & Focus: site monitoring, Good Clinical Practice, protocol, regulatory requirements, training, communication, study management, regulatory submissions, data query, project execution
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: on-site monitoring experience
Type: Full time
Benefits: Competitive salary and benefits package.

Johnson & Johnson

Skills & Focus: Site Management, Clinical Trials, GCP, Monitoring, Regulatory Compliance, Training, Data Entry, Stakeholder Management, Site Activation, Health Authority Submission
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 3-5 years
Type: Field-based