Clinical research associate

JCW Group; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A clinical research organization is seeking a Clinical Study Associate Manager to support neurology-focused clinical studies involving digital remote patient monitoring solutions. In this role, you will act as a liaison for physicians and study coordinators, develop logistics and site support processes, and maintain project documentation. The position requires clinical study operations experience, proficiency in MS Office, and strong English communication skills. Position is based in Barcelona, Spain, and is part of a long-term program support.

Formación

• Experience in clinical study operations, especially in neurology.
• Familiarity with digital clinical trials and remote patient monitoring is a strong advantage.
• Excellent communication skills in English.

Responsabilidades

• Serve as a contact for physicians and study coordinators for remote monitoring.
• Develop logistics and site support processes; manage vendors.
• Ensure prompt resolution of support requests.

Conocimientos

Clinical study operations experience

Strong communication skills in English

Proficient in MS Office (Excel, Power Point, Word)

Descripción del empleo

Clinical Study Associate Manager (Contract) – Digital / Remote Patient Monitoring

Spain - Barcelona Start : Jan / Feb

Contract : Long-term program support (6-12 months)

Industry : Neurology / Digital Clinical Trials

We are looking for several experienced Clinical Study Associate Managers to support ongoing neurology-focused clinical studies involving digital remote patient monitoring solutions. This role will be working with study sites, investigators, and internal biomarker teams to ensure smooth operational execution.

What you'll do

• Act as a point of contact for physicians and study coordinators regarding remote patient monitoring support
• Develop processes for translation, logistics and site support; select and manage vendors
• Ensure support requests are resolved quickly and effectively
• Prepare study site support materials, including training documentation
• Contribute to IRB / Ethics Committee submissions and follow-up responses
• Maintain accurate study progress dashboards (recruitment, data generation, data transfers, technical issues)
• Maintain centralized project spaces and documentation
• Support effective team communication through meeting materials and document management
• Identify opportunities to streamline processes and improve execution efficiency

Qualifications

• Clinical study operations experience, ideally in neurology
• Familiarity with digital clinical trials / remote patient monitoring (strong advantage)
• Strong communication skills in English
• Based in Spain - Barcelona
• Proficient in MS Office (Excel, Power Point, Word)