16 Biopharmaceutical Leadership jobs in São Paulo.

Hiring now: Site Care Partner Fsp @ Parexel, Assoc Mgr Global Analytic @ Iqvia, Medical Science Liaison M @ Novo Nordi, Regional Medical Mgr Esta @ Johnson Jo, Coordinator Psp Diagnosti @ Biomarin, Medical Monitor @ Psi, Sr Database Dev @ Psi Cro.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (4) Functional Service Provider (3) CRA (3) Site Care Partner (3) Project Leadership (3) stakeholders (3) data analysis (3) project management (3) Biostatistics (2) Data Management (2)

📍 Locations

São Paulo (16)

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: analytics, data mining, clinical trials, stakeholders, recommendations, communications, enrollment strategies, planning, data analysis, project management
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 of experience in clinical trials or data analysis within clinical trials.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: project management, clinical projects, communication, timelines, documentation, studies, IRB applications, invoicing, problem solving, Good Clinical Practice
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: At least 3 years of experience in project management or relevant field
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novo Nordisk

Skills & Focus: medical science liaison, social media, scientific communication, digital medical influencers, key opinion leaders, medical education, clinical research, evidence generation, treatment protocols, disease awareness
About the Company: Novo Nordisk is a dynamic company driven to change the lives of millions of patients living with diabetes and other chronic diseases. The company is focused on…
Experience: Medical degree with an active license; specialisation or clinical experience in the therapeutic area is a plus.

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.
Skills & Focus: Project Planning, Clinical Trials, Regulatory Consulting, Biopharmaceutical, Drug Development, Clinical Research, Project Leadership, Compliance, ICH Guidelines, GCP
About the Company: Parexel is a leading global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services. They help …
Type: Remote

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.
Skills & Focus: site activation, feasibility, regulatory, research, clinical, healthcare, accurate documents, project team, tracking tools, investigative sites
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: Around 1-2 years of experience working with regulatory tasks in North America
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Johnson & Johnson

Skills & Focus: Medical Affairs, pharma, strategy development, Data generation, stakeholders, business strategy, compliance, negotiation, clinical epidemiology, real world evidence
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: At least 3 years work experience in pharma industry, ideally in Medical Affairs
Type: Hybrid

Biomarin

Skills & Focus: diagnostic program, contract management, budget optimization, patient adherence, educational programs, reporting, communication skills, collaboration, pharmaceutical, biotechnology
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: A minimum of 3 years of experience in the position or similar.
Type: Hybrid

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Leadership, Compliance, Submissions, Marketing Authorization, Strategic Mindset, Cross-functional Teams, Public Health, Pharmaceutical, Biotechnology
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: At least 10 years of experience.
Type: Full-time
Skills & Focus: regulatory strategy, documentation, submissions, compliance, stakeholders, audits, registration, licenses, GMP, project management
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: 1-2 years experience in Regulatory Environment
Type: Fixed-term

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…

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.

Johnson & Johnson

Skills & Focus: Medical Manager, Rare Diseases, Medical Affairs, Pharmaceuticals, Neurology, KOLs, Strategic Thinking, Coaching, Healthcare Innovation, Patient Advocacy
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: 5 - 7 years of work experience in the pharmaceuticals industry, academic research and/or health care
Type: Hybrid