Clinical Trials Coordinator

About the Role: We are seeking a Clinical Trials Administrator to support the coordination and administration of clinical trials at ICON. The successful candidate will assist in maintaining and organizing clinical trial documentation, ensuring compliance with protocols and regulatory requirements.Key Responsibilities:Assist in the coordination and...

OverviewCDS Fortrea Inc. is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.SalaryThe estimated salary for this position is $85,000 - $110,000 per year.Job DescriptionThis Senior Clinical Trials Coordinator role involves serving as the primary contact for project teams and...

Regulatory Affairs Specialist Clinical TrialsAbout the CompanyIGC Pharma SAS is a subsidiary of a U.S. start-up clinical-stage pharmaceutical company based in New York, specializing in preventing and managing Alzheimer's and other CNS diseases. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the successful planning and...

Job Title: Clinical Trials Regional Project LeadThis exciting opportunity is within PSI, a leading organization in the healthcare industry.Job DescriptionAs a Clinical Trials Regional Project Lead, you will be responsible for coordinating activities of project teams, ensuring milestones are met, and maintaining consistency of Clinical Operations processes...

About the PositionClínica Colombia ES is seeking a highly skilled Regulatory Affairs Specialist to join our team in Bogota, Colombia. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the successful planning and execution of clinical trials and the regulatory approval of new drugs.Key Responsibilities:Regulatory Document...

About this role:As a Clinical Trials Regional Project Lead at PSI, you will play a key role in coordinating project teams and ensuring milestones are met while maintaining consistency of Clinical Operations processes across regions.Key responsibilities:Coordinate project team work and supervise clinical project team members' performance.Implement and manage...

Job Title: Clinical Trials Regional Project LeadJob Summary:We are seeking a highly skilled Clinical Trials Regional Project Lead to join our team at PSI. As a key member of our Clinical Operations department, you will be responsible for coordinating project activities, ensuring milestones are met, and maintaining consistency of Clinical Operations processes...

Are you a project management professional looking for a new challenge?We are seeking a Clinical Trials Regional Project Lead to join our team at PSI.About the RoleThe successful candidate will be responsible for coordinating activities of project teams, ensuring milestones are met and consistency of Clinical Operations processes across regions. This role...

Job Summary: We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to support our Project Team in Latin America. As a Clinical Trial Coordinator, you will provide administrative and technical support to ensure the success of our clinical trials.Key Responsibilities:Support the Project Team in coordinating and overseeing trial...

Clinical Trial Administrator Role at ICONICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to fostering an inclusive environment that drives innovation and excellence. We are proud to offer a dynamic and diverse work environment where you can contribute to shaping the future of clinical development.We are...

Job DescriptionAs a Statistical Programmer at Psi Cro, you will contribute to statistical programming activities related to global clinical trials. You will work closely with international teams of statisticians, programmers, and data managers, programming data sets and summaries.Duties and ResponsibilitiesDevelop analysis data sets structureDevelop program...

Job Title: Clinical Operations CoordinatorJob Summary:We are seeking a highly skilled Clinical Operations Coordinator to join our team at ENGINEERINGUK. As a Clinical Operations Coordinator, you will play a critical role in supporting the regional leadership governance meetings and actions, capabilities & country input for sales/PM/Feasibility/SSU, etc.Key...

**Job Summary:**Psi Cro is a leading Contract Research Organization (CRO) seeking an experienced Clinical Trials Data Programmer to join our team. As a key member of our statistical programming team, you will be responsible for developing and maintaining high-quality data sets, programs, and documentation for global clinical trials.**Responsibilities:Develop...

At PSI, we are seeking a highly skilled Clinical Trials Regional Project Lead to join our team. This is an exciting opportunity to work in a dynamic environment and take on new challenges. About the Role:The successful candidate will be responsible for coordinating project activities, ensuring milestones are met, and maintaining consistency of Clinical...

We are a dynamic, global company that cares for our staff, clients, partners, and the quality of work we do. With over 2,700 driven individuals, we work on the frontline of medical science, changing lives and bringing new medicines to those who need them.Job OverviewAs a SAS Programmer I at Psi CRO Ag, you will contribute to statistical programming...

Career Opportunities at IGC Pharma SAS: Transforming Alzheimer's ResearchJob SummaryIgc Pharma SAS, a subsidiary of a leading NYSE-listed pharmaceutical company, is seeking a highly skilled Senior Neuropsychology Researcher to join our team in Bogota. The successful candidate will play a pivotal role in the Alzheimer's disease clinical trials, driving...

Job Summary Merck Gruppe - MSD Sharp & Dohme is seeking a skilled Clinical Data Coordinator to join our team. As a Clinical Data Coordinator, you will be responsible for executing end-to-end data management activities, including data management tool and system development, validation, and maintenance. You will work closely with our team to ensure data...

About ICON and myGworkICON plc is a world-leading healthcare intelligence and clinical research organization. myGwork is the largest global platform for the LGBTQ+ business community. ICON is an inclusive employer and a member of myGwork, fostering an environment driving innovation and excellence. We welcome you to join us on our mission to shape the future...

We are seeking a skilled Clinical Trial Administrator to assist with the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.Support the preparation of study-related...

Transforming Drug and Device Development for Partners and Patients Job Description: CDS Fortrea Inc. is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Serve as the primary point of contact for project teams and investigative sites, conducting site contacts and...