Clinical Research Associate I/ Clinical Research Associate II (Oncology)

TL;DR

Clinical Research Associate I/II (Oncology): Monitor and manage progress of clinical studies at investigative sites ensuring compliance with protocols, SOPs, ICH-GCP, and regulations with an accent on oncology studies. Focus on identifying study risks, coordinating site setup activities, conducting monitoring visits, and mitigating issues.

Location: Remote based in France, preferably Paris or Paris area, with up to 50-60% domestic travel including overnight stays (international travel possible).

Company

CRO integrating clinical trial execution with scientific knowledge, laboratory expertise, and advanced data sciences, focused on Oncology and Rare Disease.

What you will do

• Monitor clinical studies at sites, ensuring conduct, recording, and reporting per protocol, SOPs, ICH-GCP, and regulations.
• Coordinate study setup activities: identify investigators, prepare regulatory submissions, conduct pre-study and initiation visits.
• Own study progress, identify risks, and propose mitigation solutions.
• Travel to sites for monitoring visits (up to 50-60% domestic, some international).

Requirements

• Life science degree or equivalent experience
• 1+ year as CRA or equivalent in CRO/pharma/biotech, site management, oncology studies experience
• Fluency in English and French (local language)
• Availability for 50-60% domestic travel with overnights
• Excellent communication, organizational skills, client-focused, team player.

Nice to have

• Study start-up activities experience.

Culture & Benefits

• High CRA retention, lower protocol load for expertise.
• Reasonable travel supporting work/life balance.
• Influence and impact in smaller CRO with direct management support.
• Amazing people and enjoyable quality of life.