[All remote jobs](https://jobicy.com/jobs.md)[![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg)](https://jobicy.com/company/precision-medicine-group.md)[Precision Medicine Group](https://jobicy.com/company/precision-medicine-group.md) # Clinical Research Associate I/ Clinical Research Associate II Review the role, location requirements, compensation details, and application process before deciding whether this opportunity fits your next career move. [Apply for this job](#job-application)[View company](https://jobicy.com/company/precision-medicine-group.md)ShareRemote from[France](https://jobicy.com/job-region/france.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished18 Oct 2026Apply before17 Nov 2026Listing views32Application actions2Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. AI Summary ## The role, at a glance. This remote-based Clinical Research Associate I/II role supports oncology and rare-disease clinical trials in France, with candidates expected to be based in the Paris area. The CRA will oversee investigative-site progress and ensure studies are conducted, documented, and reported in accordance with protocols, SOPs, ICH-GCP, and applicable regulations. Responsibilities include investigator identification, regulatory-submission support, pre-study and initiation visits, monitoring, risk identification, and site management. Candidates need a life-science degree or equivalent experience, at least one year of CRA or related clinical-research experience, oncology-study experience, and fluency in English and the local language. The position involves substantial domestic travel, including overnight stays, estimated at approximately 50–60%. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 4/5EasyHard ### Pace & Pressure 4/5RelaxedFast-paced ### Autonomy Level 4/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThe role requires regulated clinical-trial monitoring, oncology experience, strong attention to detail, and independent management of multiple investigative sites. Frequent travel and the need to identify and mitigate study risks add operational complexity. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Highly competitive$75,000US market range (per year)$65k–$85k0$93.50k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer salary was disclosed. The yearly cadence is inferred from the regular full-time Clinical Research Associate role; the displayed USD figures are estimated annual compensation benchmarks for a CRA I/II-level role and are not employer-provided pay. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial monitoring](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20monitoring.md)[Oncology clinical research](https://jobicy.com/jobs?search_keywords=Oncology%20clinical%20research.md)[ICH-GCP](https://jobicy.com/jobs?search_keywords=ICH-GCP.md)[Site management](https://jobicy.com/jobs?search_keywords=Site%20management.md)[Study start-up](https://jobicy.com/jobs?search_keywords=Study%20start-up.md)[Investigator site visits](https://jobicy.com/jobs?search_keywords=Investigator%20site%20visits.md)[Regulatory submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20submissions.md)[Clinical trial documentation](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20documentation.md)[Risk mitigation](https://jobicy.com/jobs?search_keywords=Risk%20mitigation.md)[Protocol compliance](https://jobicy.com/jobs?search_keywords=Protocol%20compliance.md)[Clinical research coordination](https://jobicy.com/jobs?search_keywords=Clinical%20research%20coordination.md)[Stakeholder communication](https://jobicy.com/jobs?search_keywords=Stakeholder%20communication.md)[Travel planning](https://jobicy.com/jobs?search_keywords=Travel%20planning.md) Sample interview questionsDescribe your experience monitoring oncology clinical trials.In my previous clinical research work, I supported oncology studies by conducting site monitoring activities, reviewing source documentation and essential documents, tracking protocol compliance, and partnering with site staff to resolve issues promptly. I understand the importance of accurate safety reporting, data quality, and timely escalation in this patient population. How do you prepare for and conduct a monitoring visit? I review the protocol, monitoring plan, prior visit reports, outstanding action items, enrollment status, and data queries before the visit. During the visit, I verify informed consent, source data, investigational product accountability where applicable, regulatory documentation, and protocol adherence, then document findings and agree on clear follow-up actions with the site. Tell us about a time you identified a study risk and helped mitigate it. I noticed that a site's delayed data entry was beginning to affect query resolution and visit readiness. I discussed the root cause with the coordinator, agreed on a prioritized data-cleaning plan, set interim checkpoints, and escalated appropriately to the study team. The site returned to expected timelines while maintaining data quality. How do you handle conflict or resistance from an investigative site? I first listen carefully to understand the site's concerns and distinguish operational constraints from compliance requirements. I communicate the rationale and patient or data-quality impact, propose practical options within the protocol and SOPs, and document agreed actions. If needed, I involve the appropriate project or line-management partners early and professionally. How do you stay organized while managing remote work and frequent travel? I use a structured planning system that prioritizes subject safety, visit schedules, critical deadlines, and outstanding site actions. I reserve time for report completion and follow-up immediately after visits, keep stakeholders updated on risks and timelines, and regularly reassess priorities as study needs change. Opportunity details ## About this role. Precision for Medicine is not your typical CRO. At Precision for Medicine 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. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully – your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. 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. About you: * 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. 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 clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will 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 * Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions) 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) * Fluency in English and for non-English speaking countries the local language of country where position based Preferred: Study start up activities experience. Please apply in English. #LI-EK1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our [Privacy Policy.](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0) For CA applicants, please also refer to our [CA Privacy Notice](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0). Precision Medicine Group 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. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com). Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com) so we can investigate and take appropriate action. Candidates must be legally authorized to work in the country of employment without employer sponsorship. Show more [Apply now >](https://jobicy.com/jobs/155681-clinical-research-associate-i-clinical-research-associate-ii.md) > Annual salary information is not provided for this position. 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