Clinical Research Associate II/ Senior Clinical Research Associate

Precision Medicine Group; France; Hybride; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking an experienced Clinical Research Associate II/Senior Clinical Research Associate for a remote position in France. The candidate should have a strong background in Oncology clinical studies, with at least one year of CRA experience. Responsibilities include monitoring clinical studies, ensuring compliance with protocols and regulations, and mentoring junior staff. This is a remote position with some travel required.

Qualifications

• CRA experience within the CRO or pharmaceutical industry, particularly in Oncology.
• Minimum 1 year of CRA experience, preferably in Oncology.
• Availability for domestic travel including overnight stays.

Responsabilités

• Monitor and own the progress of clinical studies at investigative sites.
• Coordinate activities required to set up and monitor a study.
• Support Project Managers with larger studies and train junior staff.

Connaissances

Attention to detail

Conflict resolution

Problem solving

Monitoring experience

Formation

Life science degree or equivalent experience

Description du poste

Overview

Clinical Research Associate II/ Senior Clinical Research Associate – Remote, France

Precision for Medicine is not your typical CRO. We have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. We integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences, with a strong focus on Oncology and Rare Disease. We are proud of high CRA retention rates and a culture that supports work–life balance.

We are looking for an experienced CRA II or Senior CRA to join our team in France. You will have prior monitoring experience for Oncology clinical studies in France and will be located in Paris or the Paris area.

This is a remote based position with travel to sites for monitoring visits.

About you

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared for investigator meetings, site visits or project team updates, always staying two steps ahead.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose mitigation strategies.
• You take responsibility for the quality and outcomes of your work.
• You are adept at handling conflicts using established resolution strategies.

Responsibilities

Monitor and own the progress of clinical studies at investigative sites and ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations. Coordinate activities required to set up and monitor a study (e.g., identify investigators; assist with regulatory submissions; conduct pre-study and initiation visits, etc.).

Senior CRAs oversee appropriately sized trials and support Project Managers with larger studies. Opportunities to train and mentor junior staff. Interaction with clients, initiation of payments, and involvement in proposals and client presentations.

Qualifications

Requirements:

• Life science degree or equivalent experience.
• CRA experience within the CRO or pharmaceutical industry (Oncology). Minimum 1 year of CRA experience in Oncology; titles (CRA II or Senior CRA) offered depending on experience.
• Availability for domestic travel including overnight stays; international travel may be required for some senior positions.

Preferred:

• Graduate or postgraduate degree in a scientific or healthcare discipline.
• Two+ years of oncology experience.
• Experience with study start-up activities.
• For Senior CRAs, understanding of financial management and mentoring experience.

Additional

Please apply in English.

Precision for Medicine is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.