Clinical Research Associate II (Oncology)

TL;DR

Clinical Research Associate II (Oncology): Monitoring and owning the progress of clinical studies at investigative sites with an accent on ICH-GCP compliance, site management, and oncology monitoring. Focus on coordinating study setup, identifying investigators, and mitigating potential study risks to ensure high-quality data.

Location: Must reside in Madrid or Barcelona, Spain. Includes domestic travel (up to 50-60% of the time).

Company

A specialized CRO focused on precision medicine and oncology, utilizing biomarkers and data analytics to optimize cancer therapy development.

What you will do

• Monitor and own clinical study progress at investigative sites.
• Ensure compliance with protocols, SOPs, ICH-GCP, and applicable regulations.
• Coordinate study setup, including investigator identification and regulatory submissions.
• Conduct pre-study and initiation visits.
• Identify potential study risks and propose mitigation solutions.

Requirements

• 4-year college degree or equivalent experience.
• 2+ years of experience as a CRA in a CRO or pharmaceutical/biotech industry.
• Proven experience in site management and oncology monitoring.
• Residency in Madrid or Barcelona is required.
• Fluency in English and Spanish.
• Availability for domestic travel including overnight stays (50-60% commitment).

Nice to have

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline.

Culture & Benefits

• Lower than average protocol load to enable protocol expertise.
• High CRA retention rates and a focus on reasonable travel to support work-life balance.
• High level of influence and impact within a smaller CRO environment.
• Direct support from line management.