labcorp drug development

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the...

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the...

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects. Manage and process expeditable adverse events to the required standard...

Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team! This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career...

OverviewAre you looking for that new role which combines your pharmaceutical business development experience with a company that positively impacts lives? Is the ideal company for you, one that has a compelling story to tell and is experiencing incredible global growth? Do you excel at relationship building and ultimately results? Do you act with integrity,...

Practice Manager – Industry Cloud & Digital Location: São Paulo, Brazil Role Purpose: Lead Wipro’s Industry Cloud & Digital practice in Brazil, driving cloud transformation, digital innovation, and industry‑specific solutions. Key Responsibilities Practice Leadership & Growth Define and execute the go-to-market strategy for Industry Cloud & Digital...

ABOUT US Welcome to Exela Bioscience. Headquartered in Singapore, Exela Bioscience is an SME specialty pharmaceutical company dedicated to elevating well-being through strategic excellence. We are driven by a philosophy that actively searches for and develops a value portfolio of innovative and orphan drugs. Exela Bioscience specializes in key therapeutic...

DescriptionMgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must HaveSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Publications and Scientific Communications Lead based in Brazil. Lead publication strategy and scientific communications across a portfolio of products and disease areas. This role combines strategic planning, scientific writing,...

Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have Updated: YesterdayLocation: Remote, SP, BrazilJob ID:25111443-OTHLOC-7341-2DR Description Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We...

Job SummaryJoin our dynamic team as a Pharmacovigilance Analyst in the Pharma Research & Development sector. In this role, you will play a critical part in ensuring the safety and efficacy of pharmaceutical products through the monitoring, evaluation, and analysis of drug safety data. Working closely with cross-functional teams, regulatory authorities, and...

Join an international team that accelerates drug discovery and development through scientific excellence and integrated CRO/CDMO solutions — helping our partnersRealização de análises microbiológicas diversas, preparo de meios de cultura, registros de qualidade; organização do setor.At Nuvisan, everything revolves around one central question: How can...

Overview Certara accelerates medicines using biosimulation, scientific expertise, software and technology to help biopharmaceutical companies make better drug development decisions. Our clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies around the world. The Global Account Director (GAD) is the...

Pharmacovigilance Director (FSP - Sponsor Dedicated)ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

Lead Contract ManagerSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members...

Our activities in Latin America are expanding and Medpace is seeking to add CRAs to our growing team in Brazil! The Clinical Research Associate at Medpace is offering a unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background who want to...

Job Description SummaryThe Senior Director of Risk Management within Global Pharmacovigilance provides strategic leadership and expert oversight for global product safety risk management, benefit-risk evaluation, and safety signal governance across the product lifecycle. This role ensures the highest standards of patient safety and regulatory compliance...

Job Summary : Medpace is seeking to add an experienced remote Independent Contractor for the position of CRA to our team in Brazil! The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and...

Medpace is seeking to add an experienced remote Independent Contractor for the position of CRA to our team in Brazil! The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background who...

Medpace is seeking to add an experienced remote Independent Contractor for the position of CRA to our team in Brazil! The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background who...