start up

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical...

Study Start-Up CRAICON 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, patients and suppliers.We are...

Study Start-Up CRA At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Study Start Up Associate IAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and...

Company DescriptionAbout AbbVieAbbVie's 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 including immunology, oncology and neuroscience - and products and...

Premier Research is seeking a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team. You will help transform ideas and drive start-up activities across biotech, medtech, and pharma projects, enabling timely trials and patient access.This role requires strong regulatory knowledge, English communication, and a...

Study Start Up Associate II (US experience)At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...

Company Description About AbbVie AbbVie's 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 including immunology, oncology and neuroscience - and products and...

Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives,...

Premier Research is seeking a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team. You will support global biotech and pharma sponsors by coordinating start-up activities, ensuring timelines, and maintaining regulatory alignment.You will work closely with Project Managers, Regulatory Start-up Managers, and local...

IQVIA is seeking an experienced Site Activation/Regulatory Project Manager in Argentina to oversee regulatory activities for selected studies and multi-protocol programs. You will lead pre-award activities, activation, and maintenance while managing scope, timelines, budgets and resources with cross-functional teams.This role requires coordinating with...

AbbVie seeks a Specialist, Country SSU to drive and execute start-up and maintenance activities for assigned studies and sites in their country. You will ensure on-time delivery, coordinate with CTS/Regulatory and contract teams, and support activation in IXRS while maintaining Vault SSU data.The role requires collaboration with cross-functional teams,...

Job SummaryOur 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...

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 CRA to join our diverse and dynamic team. As a Study...

Study Start Up Associate I - ArgentinaAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and...

We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring our first Senior Regulatory and Start Up Specialist (Senior RSS) in Argentina!   As the Senior RSS on our team, you are a seasoned, experienced professional in regulatory and site start-up activities. Responsibilities will be dependent upon...

We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring our first Senior Regulatory and Start Up Specialist (Senior RSS) in Argentina!   As the Senior RSS on our team, you are a seasoned, experienced professional in regulatory and site start-up activities. Responsibilities will be dependent upon...

IQVIA Biotech seeks a Sr. Site Contracts Associate in Buenos Aires with 3–5 years of sponsor or CRO experience in site contracting. You will develop grant estimates, craft contract and payment language, and support global study startup activities while ensuring regulatory compliance.Join a leading CRO offering exposure to multi-protocol programs and...