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Senior CRA (Sponsor dedicated)

Frankfurt am Main, Hessen💼 Full-time🗓 2026-05-21 → 2026-08-15

Core

Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards while ensuring data integrity and participant safety.

Role type

Senior Clinical Research Associate (Sponsor dedicated)

Builds

Clinical trials for new medicines and treatments

Domain

Healthcare / Clinical Research

Deliverable

physical/clinical work

Required skills

Clinical trial process management, regulatory compliance, site monitoring, data integrity, site performance assessment, training and guidance for site staff, stakeholder relationship management

Preferred skills

Proficiency in clinical trial software and tools, ability to manage multiple sites and projects simultaneously, problem-solving

Technologies

Clinical trial software and tools

Responsibilities

Monitoring clinical trial sites for protocol and GCP adherence, conducting site visits to assess performance and resolve issues, collaborating on data collection and reporting, providing training to site staff and CRAs, building relationships with site personnel and stakeholders

Seniority

Senior, hands-on IC

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