Last updated: 2025-05-12

11 Biopharmaceutical Leadership jobs in São Paulo.

Hiring now: Regulatory Policy Sr Mgr @ Johnson Jo, Jr Regulatory Affairs Ass @ Parexel, Sr Database Dev @ Psi Cro, Associate Proj Mgr Licens @ Iqvia, Clinical Trials Legal And @ Novo Nordi.Explore more at jobswithgpt.com. at kaamvaam.com

🔥 Skills

Regulatory Affairs (5) Consulting (4) Clinical Research (4) Drug Development (4) Project Management (3) Latin America (2) Biopharmaceutical (2) Medical Writing (2) Statistical Programming (2) Data Management (2)

📍 Locations

São Paulo (10) Campinas (1)

Johnson & Johnson

Skills & Focus: regulatory policy, advocacy plans, health authorities, Latin America, strategic policy support, collaborative team-player, regulatory trends, product development, policy developments, internal partners
About the Company: Johnson & Johnson is a company that believes health is everything and focuses on creating innovative healthcare solutions.
Experience: 2 years in regulatory or policy, 2 years in pharmaceutical company
Type: Hybrid

Parexel

Skills & Focus: Regulatory Affairs, Consulting, Biopharmaceutical, Clinical Research, Drug Development, Regulatory Consulting, Medical Writing, Statistical Programming, Data Management, Clinical Trials
About the Company: Parexel is a global biopharmaceutical services company that offers comprehensive drug development and regulatory consulting solutions across a range of therape…
Type: Full-time

Johnson & Johnson

Skills & Focus: Cell Therapy, Medical Affairs, Patient Care Coordination, Customer Service, Supply Chain, Collaboration, Case Management, Order Management, Compliance, Stakeholder Engagement
About the Company: Johnson & Johnson is a global leader in healthcare innovation, committed to improving health for humanity through scientific advancements in various medical fi…
Experience: Prior experience in customer facing role, ideally in a hospital or working with hospitals.
Type: Full-time

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: Regulatory Affairs, Medical Devices, Submissions, Licensing, Compliance, Stakeholders, Audits, Health Sector, Documentation, Brazilian Health Authorites
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: Desirable experience in Regulatory Environment; preferable in the health sector and experience with Medical Devices.
Type: Full-time

Parexel

Skills & Focus: Regulatory Affairs, Consulting, Drug Development, Clinical Research, Biopharmaceutical, Clinical Trials, Patient Safety, Regulatory Compliance, Project Management, Pharmaceuticals
About the Company: Parexel is a global biopharmaceutical services company providing comprehensive drug development and regulatory consulting services.
Skills & Focus: Regulatory Affairs, Consulting, Clinical Research, Biostatistics, Project Management, Drug Development, Healthcare, Pharmaceuticals, Patient-Centric, Global Inclusion
About the Company: Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services. They focus on adva…
Experience: Entry-level
Type: Full-time
Skills & Focus: Regulatory Affairs, Junior Role, Consulting, Clinical Research, Biopharma, Medical Writing, Data Management, Statistical Programming, Patient Focus, Global Inclusion

Iqvia

Skills & Focus: Project Management, Clinical Outcomes Assessments, Vendor Management, Financial Reporting, Pharmaceutical Industry, Drug Development, Communication Skills, Team Coordination, Contract Negotiation, Database 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: 4+ years’ work experience in clinical research, medical affairs, vendor management, or other related scientific roles. 2+ years’ work experience in a Project Management, Consulting, or other similar client facing role.
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: clinical trials, legal compliance, contract negotiation, regulatory requirements, data protection, Latin America, legal advice, risk assessment, international regulations, training
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. We are committed to expanding …
Experience: Experience working on legal, especially working with the clinical trials industry.
Type: Full-time

Johnson & Johnson

Skills & Focus: Medical Science Liaison, Healthcare, Innovative Medicine, MedTech, Scientific Knowledge, Data Integration, Stakeholder Engagement, Field Interactions, Community Relations, Medical Practice
About the Company: Johnson & Johnson is a global leader in healthcare innovation, providing a range of solutions to prevent and treat complex diseases.
Experience: At least 3 years in a relevant role
Type: Field-based