Job Overview
Location
Remote, France
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • As a Clinical Research Associate I/II at Precision Medicine Group, you will play a critical role in advancing life-changing therapies in oncology and rare diseases by ensuring clinical trials are conducted with the highest standards of quality, compliance, and scientific rigor.
- • Your day-to-day responsibilities include monitoring clinical study progress at investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and regulatory requirements; coordinating site setup activities such as investigator identification and regulatory submissions; conducting pre-study, initiation, and routine monitoring visits; and maintaining accurate documentation of all study-related activities.
- • You will join a specialized, mission-driven CRO that integrates clinical trial execution with deep scientific expertise, laboratory capabilities, and advanced data sciences—offering a collaborative environment where your input is valued and your impact is tangible.
- • This role offers the opportunity to become a protocol expert through lower-than-average protocol ownership, develop deep therapeutic area knowledge in oncology, grow your leadership and problem-solving skills, and contribute meaningfully to patient outcomes while enjoying strong work-life balance and high job satisfaction.
🎯 Requirements
- • Life science degree and/or equivalent experience
- • 1+ year of experience as a CRA in a CRO, pharmaceutical, or biotech setting, or equivalent relevant experience in clinical research/site management
- • Demonstrated experience managing oncology studies
- • Excellent communication, organizational, and interpersonal skills; ability to work effectively as a team player
- • Fluency in English and French (required for France-based role)
- • Availability for domestic travel, including overnight stays, up to approximately 50-60% of time
🏖️ Benefits
- • Lower-than-average protocol ownership enabling deep protocol expertise and reduced workload stress
- • Strong focus on work-life balance with reasonable and predictable travel requirements
- • High CRA retention rates reflecting a supportive, people-first culture and enjoyable quality of life
- • Direct access to leadership and influence in decision-making due to smaller CRO structure
- • Opportunity to work in oncology and rare disease areas with meaningful impact on patient outcomes
- • Equal Opportunity Employer commitment with accommodations available for applicants with disabilities
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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