Clinical Research Associate Job at Precision for Medicine, France | Life Sciences | Apply Now
If you are an oncology-vetted clinical monitor looking to secure a balanced lifestyle with an industry leader in precision oncology, this permanent position at Precision for Medicine is an exceptional opportunity. Linked to the regional operations hub in Paris, France, this role is home-based within the Paris area, allowing you to combine remote data management with field monitoring visits. For relationship-driven monitors searching for a high-impact Clinical Research Associate Job, this position stands out by offering a lower-than-average protocol load, reasonable regional travel, and strong line-management backing. It serves as an elite milestone for your career and represents a premier CRA Job for professionals seeking a high-growth Job in France.
- Job Position: Clinical Research Associate I/ Clinical Research Associate II
- Location: Paris, Île-de-France, France
About The Company
Precision for Medicine is a specialized, full-service clinical Contract Research Organization (CRO) dedicated to shifting the landscape of advanced cancer therapies and rare disease drug development. The company seamlessly integrates clinical trial execution with deep scientific knowledge, specialized laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients. Unlike transactional, high-turnover CROs, Precision is celebrated for its remarkably high CRA retention rates. The company builds its culture around a true work-life balance, giving monitors the breathing room needed to become genuine protocol experts whose voices are actively heard and valued by leadership.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate I or II, you will monitor and own the complete progress of targeted oncology studies at local investigative sites, ensuring absolute alignment with international and regional compliance structures.
Your core monitoring, data, and site management duties will include:
- Protocol Expert Monitoring: Overseeing clinical study execution at investigative sites to guarantee all data collection and patient safety parameters comply with the protocol, internal SOPs, and ICH-GCP guidelines.
- Study Start-Up Logistics: Coordinating vital study start-up logistics, which includes identifying potential investigators, helping prepare regulatory submissions, and executing rigorous pre-study and site initiation visits.
- Source Data Verification (SDV): Performing meticulous source data verification, checking patient informed consent logs, validating protocol eligibility, and tracking investigational product (IP) accounting at the site level for this Clinical Research Associate Job.
- Safety & Deviation Oversight: Auditing, tracking, and reporting protocol deviations or adverse events (AEs/SAEs), while applying tried-and-true resolution strategies to manage site-level conflicts.
- Risk Mitigation & Reporting: Identifying localized study risks early, constructing creative mitigation solutions, and compiling precise monitoring visit reports (MVRs) within defined corporate timelines to secure an audit-ready CRA Job.
Qualifications & Profile Requirements For Clinical Research Associate Job
This role is tailored for proactive, well-prepared monitors who stay two steps ahead of the game and possess an impeccable eye for clinical detail.
- Required Criteria:
- Educational Foundation: A formal university Life Science degree and/or equivalent clinical research experience.
- Industry Track Record: A minimum of 1 year or more of experience as a CRA within a Contract Research Organization (CRO) or pharmaceutical/biotech environment, including solid site management experience.
- Therapeutic Focus: Direct, hands-on experience managing Oncology clinical trials is required.
- Travel Commitment: Availability for domestic travel, including occasional overnight stays, constituting up to 50-60% travel commitment to investigative sites as dictated by the monitoring plan.
- Linguistic Mastery: Full fluency in both English and French (written and verbal) is required to manage international sponsor communication and local site data flows.
- Preferred Assets:
- Direct experience handling study start-up activities and regulatory submissions in France.
- Graduate or postgraduate degree with a specific concentration in an oncology-related or healthcare discipline.
In short, the Clinical Research Associate position at Precision for Medicine is a definitive route to escaping the burnout of traditional CRO networks. Securing this role allows you to step away from overloaded protocol portfolios and take real ownership of targeted, adaptive oncology trials where your insights directly optimize the development pathway. If you live in the Paris area, possess at least a year of oncology monitoring experience, and want to establish a career with a precision medicine leader, apply today to secure this premier Clinical Research Associate Job, advance a highly meaningful CRA Job, and lock in this outstanding Job in France.
