Study Start Up Manager

hace 4 días

Buenos Aires, Argentina Medpace A tiempo completo

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 Buenos Aires 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. Responsibilities Efficiently 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 Overview Medpace 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 Perks Flexible 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 Awards Recognized 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 Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr

  • Global Study Start-Up Lead

    hace 2 semanas

    Buenos Aires, Argentina ICON A tiempo completo

    A leading healthcare clinical research organization in Buenos Aires seeks a Manager, Study Start-Up. In this role, you will manage the end-to-end study start-up process, overseeing a team and ensuring compliance with regulations. Ideal candidates will have a background in life sciences, significant clinical trial experience, and strong leadership skills. The...

  • Study Start Up Manager

    hace 2 semanas

    Buenos Aires, Argentina Medpace, Inc. A tiempo completo

    Job Summary: 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 Buenos Aires! 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...

  • Study Start Up Manager

    hace 1 semana

    Buenos Aires, Buenos Aires C.F., Argentina Medpace, Inc. A tiempo completo

    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 Buenos Aires 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...

  • Start Up Manager

    hace 2 semanas

    Buenos Aires, Argentina ICON A tiempo completo

    Start Up Manager 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 Manager, Study Start‑Up to join our diverse and...

  • LATAM Study Start-Up Regulatory Manager

    hace 2 semanas

    Buenos Aires, Argentina International Flavors & Fragrances A tiempo completo

    A clinical trial management firm in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join the Study Start-Up team. This role requires at least 4 years of experience in regulatory submissions and strong communication skills. Responsibilities include managing global start-ups, quality checks on submission documents, and preparing informed...

  • Study Start Up Manager

    hace 2 semanas

    Buenos Aires, Argentina International Flavors & Fragrances A tiempo completo

    Job Summary: 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 Buenos Aires! This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous...

  • Study Start-up Associate Senior

    hace 3 días

    Buenos Aires, Buenos Aires C.F., Argentina Emmes Global A tiempo completo

    OverviewStudy Start-up Associate SeniorLATAM RemoteEmmes Group: Building a better future for us all.Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the...

  • Study Start-up Associate Senior

    hace 3 días

    Buenos Aires, Buenos Aires C.F., Argentina Emmes Group A tiempo completo

    JOB_DESCRIPTION.SHARE.HTMLCAROUSEL_PARAGRAPHJOB_DESCRIPTION.SHARE.HTMLMexico City, Mexico; Buenos Aires, Argentina; Sao Paulo, BrazilLegal / Regulatory/ComplianceYesRegular Full-Time2730Emmes Globalmail_outlineGet future jobs matching this searchorOverviewJob DescriptionStudy Start-up Associate SeniorLATAM RemoteEmmes Group: Building a better future for us...

  • LATAM Study Start-Up: Regulatory Submissions Lead

    hace 4 días

    Buenos Aires, Argentina Medpace A tiempo completo

    A leading clinical research organization in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join their Study Start Up team. This role involves managing all aspects of global start-up and requires at least 4 years of experience in regulatory submissions and strong leadership skills. You will collaborate with teams to contribute to...

  • Start-up Specialist

    hace 1 semana

    Buenos Aires, Argentina Labcorp A tiempo completo

    **Job Overview**:** Role Description Study-Start-Up/QC Specialist**: Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with...