Last updated: 2025-05-22

11 Biopharmaceutical Leadership jobs in Mexico City.

Hiring now: Clinical Research Associa @ Parexel, Especialista De Asuntos R @ Baxter, Site Activation Spec @ Syneos Hea, Regulatory Affairs Sr Spe @ Johnson Jo, Clinical Research Associa @ Psicro, Clinical Research Associa @ Psi, Associate Mgr Regulatory @ Stryker, Medical Science Liaison M @ Biogen, Rwe Lead Gbs Mexico City @ Novo Nordi, Regulatory Affairs Spec @ Teleflex.Explore more at at kaamvaam.com

🔥 Skills

Regulatory Affairs (4) Clinical Research Associate (2) CRA (2) Compliance (2) monitoring visits (2) CRF review (2) site communication (2) feasibility research (2) stakeholders (2) regulatory affairs (2)

📍 Locations

Mexico City (11)

Parexel

Skills & Focus: Clinical Trials, Clinical Research Associate, CRA, Functional Service Provider, Site Care Partner, Data Management, Biostatistics, Project Leadership, Regulatory Affairs, Statistical Programming
About the Company: Parexel is a global clinical research organization focused on providing the pharmaceutical industry with comprehensive support to develop new drugs and therapi…
Type: Full-time

Baxter

Skills & Focus: Regulatory Affairs, Sanitary Registrations, Dossier Management, Budget Management, Regulatory Indicators, Label Compliance, Record Management, Training and Compliance, Pharmacovigilance, Technovigilance
About the Company: At Baxter, we are deeply connected by our mission. Our products and therapies are found in almost every hospital worldwide, touching the lives of millions of p…
Benefits: Comprehensive benefits options reflecting the value placed on employees.

Syneos Health

Skills & Focus: Site Activation, Clinical Trial, Start-up, Regulatory, Submission, Investigational Sites, Study Specifications, Vendor Management, Contract Negotiation, Compliance
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Johnson & Johnson

Skills & Focus: Regulatory Affairs, MedTech, Regulation Sanitaria, Medicamentos, Licencias Sanitarias, Cesión de Derechos, Lifecycle Management, Matriz Compleja, Proyectos Regulatorios, Gestión de Datos
About the Company: A global healthcare company dedicated to improving health for humanity through innovative medicine and MedTech solutions.
Experience: 5+ years in Regulatory Affairs at operational level

Psicro

Skills & Focus: CRA, clinical research, monitoring visits, training, complex studies, CRF review, site communication, feasibility research, presentations, regulatory documents

Psi

Skills & Focus: Clinical Research Associate, monitoring visits, study startup, feasibility research, CRF review, source document verification, query resolution, site communication, regulatory support, study submissions

Stryker

Skills & Focus: Regulatory Affairs, COFEPRIS, Medical Devices, Submissions, Cross-functional Collaboration, Regulatory Standards, Team Management, Product Development, Compliance, Healthcare Outcomes
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes.
Experience: Previous experience in similar positions, working in Medical Devices companies, required.
Type: Full Time
Benefits: Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness …

Biogen

Skills & Focus: Medical Science Liaison, SMA, biotechnology, neuroscience, stakeholders, clinical decision-making, customer engagement, medical insights, educational initiatives, scientific excellence
About the Company: A biotechnology organization focusing on advancing medical practice within the field of neuroscience.
Skills & Focus: regulatory affairs, compliance, product launches, clinical strategies, labeling, CMC strategies, stakeholders, submissions, regulatory intelligence, Drug Regulatory Agencies
About the Company: Biogen is a global biotechnology company focused on discovering, developing, and delivering innovative therapies for people living with serious neurological di…
Type: Full-time

Novo Nordisk

Skills & Focus: RWE, cross-functional teams, project management, healthcare, life sciences, regulatory compliance, safety reporting, process optimization, team leadership, Agile
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on their strong legac…
Experience: 3 to 5 years in RWE or HEOR, 5 to 7 years in project management, leadership experience in small teams

Teleflex

Skills & Focus: regulatory affairs, medical devices, compliance, submissions, FDA, technical files, product development, global requirements, change control, project management
About the Company: Teleflex Incorporated is a global provider of medical technologies focused on improving the health and quality of people's lives through a diverse portfolio in…
Experience: 2-3 years of regulatory affairs experience in a regulated environment is required.