In-House Clinical Research Associate — Path to Traveling CRA

Rho; España; On-site; EUR 42,000 - 60,000; Full time

Benefits offered by this job

Work-life balance

Job summary

Rho is hiring an In-House Clinical Research Associate to support monitoring activities, manage CTMS data, and ensure regulatory compliance. You will work with Project Managers, traveling CRAs, and Lead CRA to assist in QA reviews, data queries, and study documentation, with opportunities to grow into a traveling CRA role.

Ideal candidates hold a life science degree and have at least 1 year of CRO/pharma experience, plus strong communication in English and local language.

Qualifications

• Bachelor's degree in life science, nursing or pharmacy fields.
• 1+ year of direct work experience managing essential documents in CRO/pharma/biotech.
• Strong communication skills in written and verbal English and local language.
• Detail-oriented with commitment to quality and regulatory compliance.

Responsibilities

• Collect, track and review investigational site records related to subject screening and enrollment.
• Assist in development of study plans and status reports.
• Collect, track and review site regulatory documents and informed consent forms.
• Interact with sites, clients, vendors and internal study teams.
• Maintain CTMS and other project tracking tools.
• Coordinate shipments of study supplies to sites and manage TMF audits.
• Support co-monitoring and remote monitoring activities; review data per guidelines.

Job description

Rho is hiring an In-House Clinical Research Associate to support monitoring activities, manage CTMS data, and ensure regulatory compliance. You will work with Project Managers, traveling CRAs, and Lead CRA to assist in QA reviews, data queries, and study documentation, with opportunities to grow into a traveling CRA role.

Ideal candidates hold a life science degree and have at least 1 year of CRO/pharma experience, plus strong communication in English and local language.