Clinical Research Associate II/ Senior Clinical Research Associate

Precision for Medicine; France; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A clinical research organization is seeking an experienced Clinical Research Associate II/Senior CRA for a remote role in France, focusing on Oncology studies. Responsibilities include monitoring clinical studies, ensuring compliance with protocols and regulations, and coordinating investigation site activities. Candidates should have a life science degree and a minimum of 1 year CRA experience in Oncology. This position offers opportunities for professional growth and requires availability for travel.

Qualifications

• Minimum of 1 year experience as a CRA in Oncology.
• CRA experience within the CRO or pharmaceutical industry.
• Availability for domestic travel; international travel may be needed for senior positions.

Responsabilités

• Monitor and manage progress of clinical studies at investigation sites.
• Ensure studies are conducted as per protocol, SOPs, and ICH-GCP.
• Coordinate setup and monitoring activities.

Connaissances

Attention to detail

Conflict resolution

Problem-solving

Ability to work under pressure

Formation

Life science degree or equivalent experience

Graduate or postgraduate degree in scientific/healthcare discipline

Description du poste

Overview

Clinical Research Associate II/ Senior Clinical Research Associate, Remote, France. Precision for Medicine is not your typical CRO. 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 emphasize high CRA retention, supportive work-life balance, and opportunities to influence projects in a smaller CRO environment.

This is a remote based position with travel to sites for monitoring visits. We are looking for an experienced CRA II or Senior CRA to join our team in France, with previous monitoring experience for Oncology clinical studies in France and a location in Paris or the Paris area.

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, and stay 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 solutions.
• You take responsibility for the quality and outcomes of your work.
• You are adept at handling conflict using tried and true resolution strategies.

How we will keep you busy and support your growth:

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

Responsibilities:

• Monitor and manage progress of clinical studies at investigation sites.
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations.
• Coordinate setup and monitoring activities (identify investigators, regulatory submissions, pre-study and initiation visits, etc.).
• Interact with clients, initiate payments, and participate in proposal activities including development and client presentations.
• Train and mentor junior staff members as appropriate.

Requirements:

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

Preferred:

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline.
• Two+ years of oncology experience.
• Study start-up activities experience would be advantageous.
• For Senior CRAs, understanding of financial management and mentoring experience would be desirable.

Other:

Please apply in English. Precision for Medicine is an Equal Opportunity Employer and maintains privacy and compliance standards across our recruitment process.