[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), [Belgium](https://jobicy.com/job-region/belgium.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished23 Oct 2026Apply before22 Nov 2026Listing views48Application actions4Application 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 Clinical Research Associate II role manages and monitors oncology clinical studies at investigative sites for a CRO focused on oncology and rare disease. The CRA will support study start-up, investigator identification, regulatory submissions, site initiation, routine monitoring, and protocol compliance. Candidates need at least two years of CRA or comparable clinical-research experience, oncology monitoring expertise, and fluency in English and Dutch. The position is remote for professionals based in Belgium or the Netherlands, with substantial domestic travel that may reach 50–60% and include overnight stays. ## 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 combines regulated clinical-trial oversight, oncology expertise, independent site management, and extensive travel. Success requires consistent accuracy across ICH-GCP, protocol, regulatory, and stakeholder requirements. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$85,000US market range (per year)$70k–$105k0$115.50k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer salary is disclosed. Estimated annual compensation is shown in USD for market-comparison purposes; the yearly cadence is inferred from this full-time Clinical Research Associate II role. ## 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 compliance](https://jobicy.com/jobs?search_keywords=ICH-GCP%20compliance.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)[Site initiation visits](https://jobicy.com/jobs?search_keywords=Site%20initiation%20visits.md)[Regulatory submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20submissions.md)[Protocol compliance](https://jobicy.com/jobs?search_keywords=Protocol%20compliance.md)[Investigator management](https://jobicy.com/jobs?search_keywords=Investigator%20management.md)[Risk mitigation](https://jobicy.com/jobs?search_keywords=Risk%20mitigation.md)[Clinical documentation](https://jobicy.com/jobs?search_keywords=Clinical%20documentation.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) Sample interview questionsHow do you ensure a clinical site remains compliant with the protocol and ICH-GCP requirements?I prepare thoroughly for each visit by reviewing prior findings, source data, enrolment status, safety information, and protocol-specific risks. During the visit, I verify critical data and processes, document findings clearly, agree corrective actions with the site, and follow up until issues are resolved. Describe how you would handle a recurring issue with source documentation at an oncology site. I would first determine the root cause through discussion with the site staff and review of the affected records. I would provide targeted training, establish a corrective and preventive action plan with clear owners and dates, document the issue appropriately, and monitor subsequent records to confirm sustained improvement. What is your experience with oncology trial monitoring, and what risks require particular attention? Oncology studies often require close oversight of eligibility criteria, tumour assessments, investigational product accountability, adverse-event reporting, concomitant medications, and time-sensitive procedures. I use the protocol and monitoring plan to prioritize these critical data and escalate risks promptly when patient safety or data integrity could be affected. How do you manage a workload involving frequent travel and multiple investigative sites? I prioritize activities according to patient safety, protocol milestones, site risk, and monitoring windows. I maintain a forward-looking visit plan, prepare site agendas in advance, complete reports promptly, and communicate early with project teams when timelines or risks require adjustment. How would you build an effective relationship with an investigator and site team? I build trust through reliable follow-through, respectful communication, and a practical understanding of site workload. I make expectations clear, listen to operational concerns, provide useful guidance, and work collaboratively to resolve issues while maintaining the required quality standards. 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 Belgium or the Netherlands. This is a remote based position with travel to sites for morning visits. We are looking for candidates based in Belgium or the Netherlands with oncology 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. * Experience managing oncology studies 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 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/156622-clinical-research-associate-ii-2.md) > Annual salary information is not provided for this position. 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