[Hiring] Clinical Research Associate I/ Clinical Research Associate II @Precision for Medicine

Role Description

We are now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in France. This is a remote based position with travel to sites for monitoring visits. We are looking for candidates based in Paris or Paris area.

• You will monitor and own the progress of clinical studies at investigative sites.
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Qualifications

• Minimum Required:
• Life science degree and / or equivalent experience.
• 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
• Site management or equivalent experience in clinical research.
• Experience managing oncology studies.
• Fluency in English and for non-English speaking countries, the local language of the country where position is based.
• Other Required:
• Excellent communication and organizational skills are essential.
• A team player.
• Evidence of a client focused approach.
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions).
• Preferred:
• Study start up activities experience.

Requirements

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility in the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.

Benefits

• Lower than average number of protocols, setting you up to be a protocol expert.
• Reasonable travel requirements.
• Support from direct line management.
• High CRA retention rates compared to industry averages.