Study Start Up Manager

1 semana atrás

São Paulo, Brasil Medpace Tempo inteiro

OverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. ResponsibilitiesEfficiently manage and successfully execute all aspects of global start-up; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and Present during bid defenses, general capabilities meetings, and audits. Qualifications***We kindly ask that you submit your CV in English*** At least 4 years of regulatory submissions/start-up management experience (leading regulatory/start-up project teams); Knowledge and experience of Clinical Trial Applications within Latam; Strong oral and written communication skills; Team oriented approach and strong leadership skills; Willing to work in an office-based model; and Fluency in English & local language Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across almost 40 countries. Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace PerksFlexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives AwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr

  • Study Start Up Manager

    4 semanas atrás

    São Paulo, Brasil Medpace Tempo inteiro

    Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...

  • Study Start Up Manager

    1 semana atrás

    São Paulo, Brasil Medpace Tempo inteiro

    OverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. ResponsibilitiesEfficiently manage and successfully execute all aspects of global...

  • Study Start Up Manager

    3 semanas atrás

    São Paulo, Brasil Medpace Tempo inteiro

    Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and...

  • Study Start Up Senior Manager-14466

    Há 3 dias

    Sao Paulo, Brasil AstraZeneca Tempo inteiro

    AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. The Study Start-up (SSU) Senior Manager has local/country responsibility for...

  • Study Start-Up Sr Manager,

    Há 2 dias

    São Paulo, Brasil Allergan Aesthetics Tempo inteiro

    Company Description AbbVie mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and...

  • Study Start-Up Sr Manager,

    18 minutos atrás

    São Paulo, Brasil Allergan Aesthetics Tempo inteiro

    Company DescriptionAbbVie mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

  • Study Start Up Associate Ii

    Há 2 dias

    São Paulo, Brasil ICON Plc Tempo inteiro

    Study Start Up Associate II - Hybrid - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Study Start Up Associate...

  • Study Start Up Associate Ii

    1 semana atrás

    São Paulo, Brasil Icon Tempo inteiro

    Study Start Up Associate II - Homebased - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Study Start Up Associate...

  • Study Start Up Associate II

    Há 7 dias

    São Paulo, São Paulo, Brasil ICON plc Tempo inteiro R$40.000 - R$80.000 por ano

    Study Start Up Associate II - Homebased - BrazilICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Study Start Up Associate II...

  • Manager, Regulatory

    Há 3 dias

    São Paulo, Brasil IQVIA Tempo inteiro

    Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions - Oversee the execution of Site Activation (including pre-award/bid defense activities)...