Research Manager with Clinical Expertise

At ICON Clinical Research, we're expanding our global Biostatistics and Programming team across Europe, seeking an experienced Principal Statistical Programmer to join this thriving group.The successful candidate will lead Phase II & III studies, creating statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables,...

About the RoleThe Clinical Project Coordinator position is a critical support role for management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets, and quality standards are achieved.This office-based position will be filled at our headquarters in Covington, KY or Raleigh, NC. Key responsibilities include:Supporting Clinical...

Come and shape the future of clinical development with ICON Clinical Research! We're currently seeking an experienced Principal Statistical Programmer to join our dynamic Biostatistics and Programming team across Europe.In this pivotal role, you'll be responsible for leading Phase II & III studies, crafting statistical programs, and analyzing data using...

Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved.Please note that this position is office based to be filled at our headquarters office in Covington, KY or the office in Raleigh, NC What...

Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. Please note that this position is office based to be filled at our headquarters office in Covington, KY or the office in Raleigh, NC.What...

Social network you want to login/join with:Clinical Research Associate (all levels), LisbonClient:Thermo Fisher ScientificLocation:Lisbon, PortugalJob Category:OtherEU work permit required:YesJob Reference:d1ced2cde3baJob Views:32Posted:23.01.2025Expiry Date:09.03.2025Job Description:At Thermo Fisher Scientific, you'll discover meaningful work that makes a...

Job OverviewIn the role of Clinical Research Specialist, you will be responsible for ensuring compliance with local and international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines for site activation activities.This position requires strong communication skills to serve as a Single Point of Contact (SPOC)...

At ICON, we're proud to foster an inclusive environment driving innovation and excellence in clinical research. As a Clinical Research Associate, you'll join the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Your Role:You will monitor multiple Phase II, III clinical trial sites, across different...

Are you passionate about shaping the future of clinical development? Join ICON Clinical Research as a Principal Statistical Programmer and become an integral part of our global Biostatistics and Programming team across Europe!You'll have the opportunity to lead Phase II & III studies, create statistical programs, and analyze data using CDISC ADaM...

Sobre o nosso clienteOur client is a pharmaceutical company with experience in various therapeutic areas.Descrição- Plan, implement, evaluate, and complete full execution of studies by setting goals and timelines- Monitor ongoing resource needs to the projects, assuring SOPs and Project Management tools will be in place- Provide monthly project status...

Job SummaryIn a rapidly growing Clinical Operations team, we are seeking Clinical Research Associates (CRAs) at all levels to be based anywhere in Portugal. As a CRA, you will play a crucial role in delivering end-to-end support for clinical trials from study start-up to monitoring through to study close-out.About the RoleWe provide end-to-end support for...

Role OverviewThe Clinical Project Coordinator is a key support role for Clinical Project Managers and Directors, ensuring the successful completion of clinical projects. This position will be based in one of our offices, either in Covington, KY or Raleigh, NC.Responsibilities include:Supporting Clinical Project Managers and Directors with project planning,...

Company OverviewThe Fundação Champalimaud is a pioneering institution dedicated to the fight against pancreatic cancer. Our state-of-the-art facilities and cutting-edge research laboratories are at the forefront of medical innovation.Job DescriptionWe are seeking a highly skilled Clinical Research Nurse Specialist to join our multidisciplinary team. As a...

Social network you want to login/join with:Senior Clinical Research Associate - Sponsor Dedicated - based in Portugal, LisbonClient:IQVIALocation:Lisbon, PortugalJob Category:OtherEU work permit required:YesJob Reference:e66c20481d94Job Views:47Posted:23.01.2025Expiry Date:09.03.2025Job Description:Senior Clinical Research AssociateIQVIA is the Human Data...

.- Job title: Medical Affairs Clinical Research Advisor- Location: Lisbon (Portugal)MISSION:The main mission of the Medical Affairs Clinical Research Advisor (MACRA) in Portugal is to:Capture the R&D, Medical Affairs, and local Business Units needs, to ensure transversal alignment for the conduct of Clinical Trials in Portugal.Support the local R&D activity...

Company Overview:At Thermo Fisher Scientific, we strive to make a positive impact on a global scale. Our mission is to enable our customers to make the world healthier, cleaner and safer.We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of...

Job DescriptionSenior Clinical Research Associate Role at IQVIA PortugalThis role is for a Senior Clinical Research Associate to work closely with a client in Portugal. The ideal candidate will have strong knowledge of clinical research and regulatory requirements.Your Key ResponsibilitiesConduct site selection, initiation, monitoring, and close-out...

Join Fortrea as a Clinical Research Associate (CRA2) - This role is for upcoming future opportunities that may arise at Fortrea.Job OverviewAs a CRA, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You'll have the autonomy to manage sites and drive study...

About the RoleWe are seeking a highly skilled Regulatory Manager for Clinical Trials to join our team at IQVIA LLC. As a key member of our regulatory management group, you will be responsible for overseeing complex clinical trial projects or programs.Key ResponsibilitiesAct as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or...

Senior Clinical Research Associate - Sponsor Dedicated - based in PortugalIQVIA is the Human Data Science Company oriented to drive human health outcomes forward.When you join IQVIA Portugal as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our...