Associate Manager, Clinical Trials Regulatory Management

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

Descripción de la vacante

A clinical research organization is seeking experienced Clinical Study Associate Managers based in Barcelona, Spain, to support neurology-focused clinical studies involving digital remote patient monitoring solutions. Responsibilities include acting as a liaison for study coordinators, developing support processes, and maintaining study dashboards. Strong communication and clinical study operations experience are essential for this role.

Formación

• Experience in clinical study operations, ideally in neurology.
• Familiarity with digital clinical trials or remote patient monitoring is a strong advantage.
• Strong communication skills in English.

Responsabilidades

• Act as a point of contact for physicians and study coordinators.
• Develop processes for translation, logistics, and site support.
• Maintain accurate study progress dashboards.

Conocimientos

Clinical study operations experience

Familiarity with digital clinical trials

Strong communication skills

Proficient in MS Office

Descripción del empleo

Clinical Study Associate Manager (Contract) – Digital / Remote Patient Monitoring Spain - Barcelona ⏱ Start : ASAP Contract : Long-term program support Industry : Neurology / Digital Clinical Trials

We are looking for 2 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

You should have

• 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, PowerPoint, Word)