Global Clinical Trials Assistant

Join us as a Clinical Trials Assistant! - What You´ll DoPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...

**Join us as a **Clinical Trials Assistant!**: **What You´ll Do** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...

Job OverviewThe Global Clinical Supplies Specialist will play a pivotal role in ensuring the seamless execution of clinical trials. Reporting to the Director of Clinical Supplies, this individual will be responsible for managing all aspects of clinical supplies logistics, from planning and coordination to delivery and distribution.

**Job Overview** Support Clinical Research Associates and Regulatory teams in administrative tasks to ensure accurate Trial Master File. **Key Responsibilities** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that...

Join us as a Clinical Trials Assistant! - What You´ll DoPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...

Are you looking for a challenging role in clinical operations where you can utilize your expertise to drive the success of clinical trials?About the RoleWe are seeking an experienced Global Clinical Operations Manager to join our team. In this role, you will be responsible for leading regional/global clinical trial management activities for internally...

**Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a...

Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. **Job Title** Clinical Operations Specialist At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life - changing medicines to patients. We are seeking...

**Join us as a **Clinical Trials Assistant!**: **What You´ll Do** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team of professionals in this key role. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials across various therapeutic areas.The ideal candidate will possess excellent communication skills, attention to detail, and the...

As a leading global contract research organization (CRO), SAO Fortrea Brazil Limitada provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.The Central Monitoring Lead is responsible for the execution of key Central...

Seeking a highly motivated and detail-oriented Clinical Trials Coordinator to join our team at CDS Fortrea Inc. in New Roles.About the Role:We are looking for a skilled professional with experience in logistics, imports, and supplies within a contract research organization (CRO) environment.The successful candidate will be responsible for coordinating...

**Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a...

About TFS HealthScienceTFS HealthScience is a leading Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies worldwide. Our expertise includes full-service capabilities, resourcing solutions, and functional service delivery across various therapeutic areas.We are currently seeking a Clinical Development Specialist...

At PSI, we are seeking an experienced Clinical Trials Regional Project Manager to join our team. Job OverviewThis is a key role that requires strong project management skills and experience in the clinical trials industry.ResponsibilitiesThe successful candidate will be responsible for coordinating activities of project teams, ensuring milestones are met,...

Job Overview PSI is seeking a highly skilled Clinical Trials Quality Assurance Specialist to join their team. This role will involve ensuring high-quality standards within clinical trials and internal company processes. Key Responsibilities Planning, conducting, and reporting of QA auditsCommunicating with project teams regarding QA study auditsAssembling...

Transforming Clinical Trials with FortreaBUE Fortrea Argentina S.A. is a leading global contract research organization (CRO) dedicated to delivering cutting-edge clinical development solutions across multiple therapeutic areas.As a Clinical Development Specialist II, you will be part of our team that revolutionizes the drug and device development process,...

About the Role">This role is a fantastic opportunity to lead a centralized monitoring team in clinical trials. If you have experience in project oversight, quality assurance, and risk management, we encourage you to apply.">Key Responsibilities">Project Oversight: Oversee clinical deliverables on assigned projects, manage project resources, and coordinate...

At BUE Fortrea Argentina S.A., we're a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. Our team provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across over 20 therapeutic...

We are looking for a Investigator Payments Assistant to join our Global team! (Fixed term 6 months) Home base Essential Functions Manages end-to-end investigator payment process including the coordination and facilitation of grants to investigators involved in clinical trials. Partners with clinical operations teams and IT organization to align electronic...