Project Management Specialist Clinical Trials

Company OverviewIQVIA Argentina is a leading provider of data management solutions for clinical trials. Our team of experts provides high-quality services to clients worldwide.Job DescriptionWe are seeking a highly experienced and skilled Data Management Director to join our team. The successful candidate will have a proven track record in managing data...

About the RoleWe are seeking a highly experienced Clinical Data Governance Specialist to join our Real World Evidence team. As a key member of the team, you will be responsible for leading the Clinical Data Management (CDM) team, providing expertise and vision in project planning, execution, and close-out.ResponsibilitiesOversee the delivery of high-quality...

Key ResponsibilitiesThis Principal Clinical Data Science Lead will manage fast-moving early phase studies or programs of studies to ensure project objectives are met within budget, to agreed timelines, and to a high level of quality. You'll work closely with Clinical Operations, Biostatistics, SAS Programming, Medical Writing, and Quality Assurance to ensure...

Merck Gruppe - MSD Sharp & Dohme is seeking a highly skilled Clinical Safety Specialist to support safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development.The ideal candidate will assist the protocol lead in safety reporting activities for...

About the RoleWe are seeking an experienced Associate Director of Data Management to join our team at MSD. In this role, you will be responsible for leading Senior clinical data managers and Clinical Data Managers in operations tasks within a Data Management Center. The successful candidate will have a strong background in Clinical Trials and experience in...

Job DescriptionWe are seeking a highly skilled Clinical Research Associate to join our team at Merck Gruppe - MSD Sharp & Dohme. As a key member of our global clinical research operations, you will play a critical role in ensuring the success of our clinical trials.Key Responsibilities:Develop and maintain strong relationships with investigators and site...

As a member of MSD’s clinical research team, you will play a critical role in ensuring the successful execution of clinical trials. The Clinical Research Manager will be responsible for managing the day-to-day activities of assigned protocols, including project planning, site management, and quality control.Key Responsibilities:Main Point of Contact (POC)...

Key Responsibilities:Team Leadership: Supervise data operations teams, provide oversight, and ensure project milestones are met within designated timelines.Service Management: Collaborate with stakeholders to define project scope, objectives, and deliverables.Documentation and Reporting: Maintain accurate project documentation, generate project-related...

**Practicante** **Clinical Trial Operations** - **Finanzas**¿Estás listo para poner en práctica tus conocimientos, aprender e impactar en millones de vidas?Si es así, esta es la oportunidad perfecta para que hagas parte de una empresa que le apuesta a la innovación, la experimentación y el crecimientoEl practicante de Global Clinical Trial Operations...

We are seeking a skilled and experienced Project Management Specialist to join our team at ALLSTARSIT. As a key member of our organization, you will play a crucial role in planning, facilitating, and executing projects for our clients.The ideal candidate will have a proven track record of delivering projects on time, within budget, and to the highest quality...

This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a particular study for...

Key Responsibilities:Deliver high-quality Site Management project tasks, providing guidance and advice to achieve exceptional performance.Ensure overall project efficiency, adherence to timelines, and financial goals; report metrics and out-of-scope activities.Develop and implement Site Recruitment, SPS Operations, and SPS Risk Management Plans within the...

Pursue a challenging career as an IT Project Management Specialist at Patagonian. In this role, you will oversee the entire project lifecycle, from initiation to deployment. Develop your skills in project coordination, stakeholder management, and team leadership.Key ResponsibilitiesDevelop and maintain project schedules, resource allocation plans, and budget...

Responsibilities:Ensuring effective time management, organizational, and interpersonal skills, conflict management, problem-solving skills.Able to work highly independently across multiple protocols, sites, and therapy areas.High sense of accountability/urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.Core...

Maintaining the highest level of quality and integrity in clinical trials requires a Pharmaceutical Clinical Safety Professional with expertise in safety reporting.MERCK Gruppe - MSD Sharp & Dohme is searching for an experienced professional to support safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational...

As a LIFT Field Trials Specialist at GlobalLogic, you will play a critical role in supporting client lab integration, testing, qualifications, and field trials. You will design and implement IP networking ecosystems with our platform/system to support client use cases.About the Role:You will work with a leading provider of innovative broadband solutions that...

Job DescriptionThe Clinical Research Coordinator will be responsible for the comprehensive administration of clinical trials and sites under the oversight of the line-manager.This role involves preparing, collating, distributing and archiving clinical documents. The coordinator must ensure that all trial and site-related tasks are completed in a timely...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Merck Gruppe - MSD Sharp & Dohme. As a key member of our global clinical research operations, you will play a critical role in ensuring the success of our clinical trials.Main Accountabilities:Ensure compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations,...

Job ProfileThe Clinical Operations Manager will oversee the administration of clinical trials and sites, ensuring that all tasks are completed in a timely manner to meet planned Site Ready dates.Main Tasks:Document Management:Preparation and distribution of clinical documents, including eTMF.Collation and archiving of clinical documents.eTMF reconciliation...

Job SummaryThe Regulatory Compliance Specialist will be responsible for ensuring that all clinical trials and sites comply with regulatory requirements and guidelines.Main Duties:Document Management:Preparing and distributing clinical documents, including eTMF.Collating and archiving clinical documents.eTMF reconciliation and quality control.Updating manuals...