Empleos de clinical study coordinator en Cuenca

Clinical Research Coordinator in Toledo Working Hours: 20-24 hours per week Start Date: Immediately Duration: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique opportunity to contribute to meaningful research in a...

Responsibilities(a) Site management - Study site selection, initiation (SIV) and clinical monitoring. - Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. - Prepare and conduct SIV to ensure adequate study training for relevant site...

Ready for your next career move? With continued business growth and a strong pipeline of new projects, Veramed is creating new opportunities for Statistical Programmers to work on innovative studies, expand their skills and advance their careers within a supportive, specialist CRO We have multiple exciting opportunities for Principal and Senior level...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview Join Precision for Medicine as a Clinical Project Manager/Senior CPM to lead end‐to‐end global oncology trials in a CRO environment. You will drive project delivery, manage cross‐functional teams, and maintain client relationships, budgets, and timelines from proposal through study completion. You'll ensure quality and coordination across...

Overview In this role you lead global clinical trial activities to ensure on-time delivery and high-quality results within Parexel's sponsor-driven environment. You guide cross‐functional trial teams, manage timelines and budgets, and ensure regulatory compliance across regions. You partner with internal and external stakeholders to translate strategy...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview In this role you will lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview As Global Study Manager (Oncology) you will lead interdisciplinary clinical programs from proposal to final deliverables, ensuring GCP compliance and financial performance. You'll act as the primary liaison with customers to launch, run, and close studies within contractual scopes. You'll guide cross-functional teams, manage timelines, and mentor...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview In this CRA role, you will lead clinical monitoring at trial sites to ensure quality data and adherence to ICH-GCP and local regulations. You will collaborate with regional operations to meet study milestones and identify gaps for CAPA. The position supports site start-up, training, and ongoing oversight in oncology/hematology trials. You will...

Overview In this role you ensure robust clinical trial compliance at country and site levels within an oncology-focused research landscape. You work with country, regional, and global teams to safeguard patient safety, data integrity, and inspection readiness. You apply a risk-based approach to identify and manage compliance risks and influence study...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview In this role you ensure high-quality clinical data for sponsor-led trials, working remotely across Poland, Spain or the UK. You will review patient data, resolve data inconsistencies, and support data-cleaning activities ahead of analyses, collaborating with cross-functional teams to meet GCP and protocol requirements. You will help maintain data...

Overview In this role you drive late-phase oncology development by turning scientific strategy into executable clinical trials. You lead protocol execution, data quality, and cross-functional collaboration to produce decision-ready data that informs regulatory decisions. You will be a scientific expert across the therapeutic area, guiding investigators,...

Overview In this role you will guide late-phase Hematology/Immunology trials as a sponsor-side Clinical Project Manager II. You'll coordinate with CROs and vendors, drive study timelines, and oversee documentation and risk management. This position offers global scope and a chance to shape pivotal studies within a mission-driven organization. ...

Overview In this Global Clinical Project Manager II role, you will support late-phase Hematology and Immunology trials for sponsor programs. You will liaise with CROs and vendors, keep the project team aligned on timelines, and contribute to study documents and risk templates. You'll drive end-to-end trial execution from start-up through close-out,...

Overview In this role you will oversee site management, clinical and central monitoring to safeguard patient safety, data integrity, and regulatory compliance. You will manage activities from activation to closeout, coordinate with cross-functional teams, and apply risk-based approaches to keep trials on track. You will engage with investigators and sites,...