Clinical Research Associate I/II (Oncology)

TL;DR

Clinical Research Associate I/II (Oncology): Monitoring and managing clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards with an accent on oncology and rare disease trials. Focus on conducting site visits, coordinating regulatory submissions, and mitigating study risks to ensure high-quality data reporting.

Location: Remote based in France; must be based in Paris or Paris area; requires domestic travel (approximately 50-60%).

Company

hirify.global is a CRO that integrates clinical trial execution with deep scientific knowledge, with a strong focus on Oncology and Rare Diseases.

What you will do

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted and reported per protocol, SOPs, ICH-GCP, and all applicable regulations.
• Coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
• Conduct pre-study and initiation visits.
• Identify potential study risks and propose mitigation solutions to ensure quality outcomes.

Requirements

• Life science degree and/or equivalent experience.
• 1+ year of experience as a CRA in a CRO, pharmaceutical, or biotech industry.
• Proven experience managing oncology studies.
• Fluency in English and French is required.
• Must be based in Paris or the Paris area.
• Availability for domestic travel including overnight stays (50-60% commitment).

Nice to have

• Experience with study start-up activities.

Culture & Benefits

• Lower than average number of protocols per CRA, allowing for deeper expertise.
• Reasonable travel requirements to support better work-life balance.
• High CRA retention rates and a supportive direct line management structure.
• Opportunity to have a tangible influence and impact within a smaller CRO environment.