Empleos de clinical study coordinator en Murcia

Se busca Coordinador de Estudios Clínicos para ensayo fase III en salud de la mujer en Madrid. El puesto implica gestión del estudio, coordinación de pacientes, manejo de datos y documentación, y cumplimiento de normativas. Requiere experiencia en ensayos clínicos y conocimiento de GCP. Contrato de 18 meses.

Study Site Specialist – SpainWe are seeking an experienced Study Site Specialist to join a global clinical resSearch programme. This is a permanent, fully remote position for candidates based in Spain.Location: SpainWorking arrangement: Fully remoteEmployment type: PermanentPosition SummaryThe Study Site Specialist will manage site start-up activities in...

Clinical Study Lead, Precision MedicineRevise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción.2 positions | New role within MDx CRO's Precision Medicine teamAbout the roleMDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances...

Clinical Study Lead, Precision Medicine2 positions | New role within MDx CRO's Precision Medicine teamAbout the roleMDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team.This is not a conventional CRA role. It is not a purely regulatory role either.It sits where biomarker science, investigational...

Clinical Study Lead, Precision Medicine2 positions | New role within MDx CRO's Precision Medicine teamAbout the roleMDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team.This is not a conventional CRA role. It is not a purely regulatory role either.It sits where biomarker science, investigational...

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team. This is not a conventional CRA role. It is not a purely regulatory role either. It sits where biomarker science,...

Study Site Specialist – Spain We are seeking an experienced Study Site Specialist to join a global clinical res Search programme. This is a permanent, fully remote position for candidates based in Spain. Location: Spain Working arrangement: Fully remote Employment type: Permanent Position Summary The Study Site Specialist will manage site start-up...

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...

Tigermed is seeking a Clinical Research Associate to oversee study site selection, initiation, monitoring, and safety reporting in compliance with protocol and ICH-GCP guidelines. The role includes coordinating materials, training site staff, and ensuring timely documentation throughout the study lifecycle.The ideal candidate will have a Bachelor degree or...

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 staff to proceed with study start and conduct in...

Programmer (SAS & R) with German - Spain-based (remote/hybrid)Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid)Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Overview As a Project Director, you lead global oncology clinical trial programs, overseeing study portfolios and cross-functional teams to ensure on-time, within-scope delivery. You partner with clients to align on goals, drive process improvements, and maintain high-quality execution across studies. You shape trial strategy, risk management, and change...

Programmer (SAS & R) with German - Spain-based (remote/hybrid)Desplácese hacia abajo para ver todos los requisitos del puesto y las responsabilidades que pueden esperar los candidatos seleccionados.Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG)...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

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,...

Principal Biostatistician | Global CRO | Home Based | Spain | Permanent |We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across...

Principal Biostatistician | Global CRO | Home Based | Spain | Permanent |We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across...