[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 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[Netherlands](https://jobicy.com/job-region/netherlands.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished18 Oct 2026Apply before17 Nov 2026Listing views38Application 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. Precision for Medicine is seeking a Clinical Research Associate II to remotely support clinical trial sites in the Netherlands. The role owns site monitoring and study progress, ensuring trials 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, risk identification, and site management. Candidates need a life-science background or equivalent experience, at least two years of CRA or relevant clinical research experience, fluency in Dutch and English, and availability for substantial domestic travel. Oncology monitoring and study start-up experience are advantageous. ## 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 insightThis role requires independent oversight of regulated clinical research activities, detailed protocol and ICH-GCP compliance, and proactive management of site-level risks. Frequent travel and coordination with investigators, clients, and internal study teams add operational complexity. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$90,000US market range (per year)$75k–$110k0$121.00k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer compensation was disclosed. The yearly cadence and estimated USD market range are inferred for a full-time CRA II position; these are AI estimates rather than verified employer pay or salary research. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial monitoring](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20monitoring.md)[ICH-GCP](https://jobicy.com/jobs?search_keywords=ICH-GCP.md)[Site management](https://jobicy.com/jobs?search_keywords=Site%20management.md)[Clinical research](https://jobicy.com/jobs?search_keywords=Clinical%20research.md)[Study start-up](https://jobicy.com/jobs?search_keywords=Study%20start-up.md)[Regulatory submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20submissions.md)[Investigator site visits](https://jobicy.com/jobs?search_keywords=Investigator%20site%20visits.md)[Protocol compliance](https://jobicy.com/jobs?search_keywords=Protocol%20compliance.md)[Risk management](https://jobicy.com/jobs?search_keywords=Risk%20management.md)[Oncology clinical trials](https://jobicy.com/jobs?search_keywords=Oncology%20clinical%20trials.md)[SOP compliance](https://jobicy.com/jobs?search_keywords=SOP%20compliance.md)[Dutch language](https://jobicy.com/jobs?search_keywords=Dutch%20language.md)[English language](https://jobicy.com/jobs?search_keywords=English%20language.md)[Stakeholder communication](https://jobicy.com/jobs?search_keywords=Stakeholder%20communication.md)[Clinical documentation](https://jobicy.com/jobs?search_keywords=Clinical%20documentation.md) Sample interview questionsHow do you ensure that a clinical trial site remains compliant with the protocol, ICH-GCP, and applicable regulations?I prepare thoroughly before each visit by reviewing prior monitoring reports, outstanding action items, enrollment data, and protocol requirements. During the visit, I verify source data, informed-consent documentation, investigational product accountability, and essential documents, then document findings clearly and agree on realistic corrective actions with the site. Describe a time you identified a potential study risk and how you addressed it. I would assess the risk's likely impact on participant safety, data integrity, and study timelines, gather the relevant evidence, and escalate through the appropriate study-team channels. I would work with the site on a documented mitigation plan, set follow-up dates, and confirm that corrective actions were effective. How do you manage competing priorities when you are responsible for several investigative sites? I prioritize activities according to patient safety, critical data, upcoming milestones, monitoring frequency, and the severity of open issues. I maintain a structured visit and action-item plan, communicate early when risks emerge, and keep sites and project stakeholders informed of timelines and dependencies. What is your approach to building effective relationships with investigators and site staff? I aim to be prepared, responsive, respectful, and clear about expectations. By understanding each site's workflow, providing practical guidance, and following through on commitments, I can build trust while maintaining the appropriate independence needed for compliance oversight. What experience do you have with study start-up activities? I understand that effective start-up requires careful investigator and site assessment, collection and review of essential documents, regulatory submission support, and well-organized initiation visits. My focus would be to confirm site readiness, clarify protocol requirements, and ensure staff have the resources and training needed before enrollment begins. 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 II to join our team in the Netherlands. This is a remote based position with travel to sites for morning visits. We are looking for candidates based in the Netherlands with biopharma monitoring experience. 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 * 2 years 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. * 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, Dutch * French will be a plus * oncology monitoring experience will be a plus 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/155683-clinical-research-associate-ii.md) > Annual salary information is not provided for this position. 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