Empleos de research associate en Barcelona

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this role you will lead and oversee clinical trial monitoring as a senior CRA within Alira Health’s global Clinical team. You will work independently and with cross-functional partners to ensure protocol compliance, quality, and timely site visits across Spain and Europe. You will shape monitoring plans, mentor junior CRAs, and collaborate...

Research Associate, UNSW CanberraAunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren.Employment type: Fixed-term contract, full-timeDuration: 2 yearsRemuneration: Level A6 $118,467 + leave loading + 17%...

Overview In this role you work within IQVIAs sponsor-dedicated team to support clinical trial operations across multiple therapeutic areas. You will conduct site visits, help develop recruitment plans, and ensure site practices meet GCP/ICH standards. You will track regulatory submissions, recruitment, CRF completion, and data queries while collaborating...

Overview In this full-time, home-based CRA role in Barcelona, you support patients and sites as Medpace accelerates the development of pharmaceuticals and medical devices. You join a training-focused program (PACE) to build independent CRA expertise through hands-on practice and rotations. The role offers diverse therapeutic exposure, cross-functional...

Overview You will support clinical development as a site-focused CRA across multiple therapeutic areas from home-based Spain. You'll drive site monitoring, ensure GCP/ICH compliance, and manage data quality while coordinating with cross-functional teams. The role blends investigator relations, regulatory tracking, and TMF/ISF maintenance to sustain study...

Clinical Research Associate Home based MadridAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...

OverviewIn this CRA II role, you support sponsor-driven clinical trials from a global, collaborative CRO. You will monitor sites, ensure data integrity and patient safety, and work with investigators to enable compliant study conduct. The position emphasizes independent yet cross-functional collaboration within a fast-paced environment. You contribute to...

Clinical Research Associate Home based BarcelonaAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...

Clinical Research Associate Home based BarcelonaAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will...

Overview En esta posición apoyarás la monitorización de ensayos clínicos de fases II–III para una empresa del sector farmacéutico/CRO con presencia nacional e internacional. Trabajarás en Barcelona desde un modelo híbrido, colaborando con centros hospitalarios y equipos clínicos para asegurar cumplimiento y calidad de los datos. Te enfrentarás a...

Overview You will support clinical development as a site-focused CRA across multiple therapeutic areas from home-based Spain. You'll drive site monitoring, ensure GCP/ICH compliance, and manage data quality while coordinating with cross-functional teams. The role blends investigator relations, regulatory tracking, and TMF/ISF maintenance to sustain study...

Overview En esta posición apoyarás la monitorización de ensayos clínicos de fases II–III para una empresa del sector farmacéutico/CRO con presencia nacional e internacional. Trabajarás en Barcelona desde un modelo híbrido, colaborando con centros hospitalarios y equipos clínicos para asegurar cumplimiento y calidad de los datos. Te enfrentarás a...

Overview As a Junior CRA at IQVIA Spain, you will support sponsor-directed clinical studies across therapeutic areas, gaining hands-on experience in site management and regulatory processes. You will work with study sites and client teams to ensure high-quality trial execution and data integrity. This role offers growth within a stable, international...

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Overview In this full-time, home-based CRA role in Barcelona, you support patients and sites as Medpace accelerates the development of pharmaceuticals and medical devices. You join a training-focused program (PACE) to build independent CRA expertise through hands-on practice and rotations. The role offers diverse therapeutic exposure, cross-functional...

Overview In this role you work within IQVIAs sponsor-dedicated team to support clinical trial operations across multiple therapeutic areas. You will conduct site visits, help develop recruitment plans, and ensure site practices meet GCP/ICH standards. You will track regulatory submissions, recruitment, CRF completion, and data queries while collaborating...

Overview You will support clinical development as a site-focused CRA across multiple therapeutic areas from home-based Spain. You'll drive site monitoring, ensure GCP/ICH compliance, and manage data quality while coordinating with cross-functional teams. The role blends investigator relations, regulatory tracking, and TMF/ISF maintenance to sustain study...

Overview In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with...

Company DescriptionPSI is a leading Contract Research Organisation with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionAs a Clinical Research Associate I you will work...