[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) # CRA II/ SCRA 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[Poland](https://jobicy.com/job-region/poland.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished26 Oct 2026Apply before25 Nov 2026Listing views76Application 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 is a senior-level clinical research monitoring role supporting oncology trials for a CRO in Poland. The CRA II/SCRA independently manages investigative sites from initiation through close-out, with responsibility for site quality, risk identification, patient safety, data integrity, and regulatory compliance. The role requires at least three years of independent monitoring experience and prior oncology trial monitoring experience. It is fully home-based but involves substantial domestic travel, including overnight stays, of approximately 50–60%, with occasional international travel. The successful candidate will work closely with CTMs, study teams, investigators, and potentially clients while contributing to issue resolution and process improvements. ## 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 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThe role requires independent oversight of complex oncology sites, sound judgment on patient-safety and data-integrity risks, and knowledge of ICH-GCP and regulatory requirements. High travel volume, competing site priorities, and direct escalation responsibilities add to the operational complexity. ## 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–$110k0$121.00k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. The employer did not disclose compensation. The yearly cadence is inferred from this regular full-time professional CRA II/SCRA role. Estimated annual market compensation is shown in USD for editorial benchmarking and may differ materially based on Polish payroll arrangements, seniority, therapeutic-area expertise, and travel expectations. ## 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 trials](https://jobicy.com/jobs?search_keywords=Oncology%20clinical%20trials.md)[ICH-GCP](https://jobicy.com/jobs?search_keywords=ICH-GCP.md)[Site initiation visits](https://jobicy.com/jobs?search_keywords=Site%20initiation%20visits.md)[Site close-out visits](https://jobicy.com/jobs?search_keywords=Site%20close-out%20visits.md)[Site management](https://jobicy.com/jobs?search_keywords=Site%20management.md)[Risk identification](https://jobicy.com/jobs?search_keywords=Risk%20identification.md)[Patient safety](https://jobicy.com/jobs?search_keywords=Patient%20safety.md)[Data integrity](https://jobicy.com/jobs?search_keywords=Data%20integrity.md)[Clinical trial compliance](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20compliance.md)[Investigator relationship management](https://jobicy.com/jobs?search_keywords=Investigator%20relationship%20management.md)[Protocol compliance](https://jobicy.com/jobs?search_keywords=Protocol%20compliance.md)[CTM collaboration](https://jobicy.com/jobs?search_keywords=CTM%20collaboration.md)[Polish and English fluency](https://jobicy.com/jobs?search_keywords=Polish%20and%20English%20fluency.md) Sample interview questionsHow do you prioritize monitoring findings when several issues are identified at a clinical site?I assess each finding against patient safety, subject rights, data integrity, protocol impact, and regulatory risk. I address critical issues immediately, document the rationale and actions clearly, escalate when required, and establish a follow-up plan with the site and study team. Describe how you would manage a site that is repeatedly late with data entry and query resolution. I would first review the underlying trends and discuss root causes with the coordinator and investigator. I would agree on a realistic corrective action plan with specific milestones, provide focused guidance where needed, document the discussion, and escalate to the CTM if progress remains insufficient or trial timelines are at risk. What are the key considerations when monitoring an oncology trial, particularly an early-phase study? I focus closely on informed consent, eligibility confirmation, safety reporting, investigational product accountability, protocol-required assessments, dose modifications, and timely documentation of adverse events. In early-phase studies, rapid communication and careful review of safety and dose-escalation data are especially important. How do you ensure that you remain compliant with ICH-GCP while working independently from home and travelling between sites? I use structured monitoring plans, current study documents, visit preparation checklists, and timely follow-up documentation. I maintain clear communication with the CTM and study team, complete required training, and escalate uncertainties early so that decisions are documented and aligned with the protocol, SOPs, and applicable regulations. Give an example of how you would raise a sensitive compliance issue with an investigator. I would present the issue factually, explain its potential effect on participants, data, or regulatory compliance, and listen to the investigator's perspective. I would keep the discussion solution-oriented, agree on corrective actions and deadlines, document the outcome, and involve the CTM or appropriate functions if escalation is necessary. Opportunity details ## About this role. Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. Our CRAs work with a manageable study portfolio, allowing them to build deep protocol and site knowledge rather than spreading their focus across too many studies. With reasonable travel expectations, accessible line management and a smaller CRO environment, experienced CRAs have the autonomy to make decisions, influence how studies are delivered and see the impact of their work. Precision for Medicine is recruiting a Clinical Research Associate II / Senior Clinical Research Associate to join our full-service team in Poland. ** This position is fully home based ** About you: * You are an experienced independent monitor who takes ownership of your sites and does not wait to be told what needs attention. * You understand what really matters for patient safety, data integrity and study delivery, and can distinguish critical risks from administrative noise. * You build credible relationships with investigators and site teams while remaining confident in addressing difficult or sensitive issues. * You identify emerging risks early, escalate appropriately and come with solutions, not just problems. * You are organized and well prepared, able to manage competing priorities across your sites without compromising quality. * You communicate clearly with CTMs and study teams and can confidently represent the site perspective in project discussions. * You take responsibility for the quality and outcomes of your work. How we will keep you busy and support your growth: You will independently manage and monitor investigative sites, taking ownership of site performance, quality and risk identification from site initiation through close-out. You will partner closely with CTMs and study teams to anticipate issues, drive timely resolution and ensure studies are conducted, recorded and reported in accordance with the protocol, SOPs, ICH-GCP and applicable regulatory requirements. You may also interact directly with clients and support site payment activities. Depending on your experience, you may have the opportunity to mentor less experienced CRAs and contribute your expertise to study-level discussions and process improvements. Qualifications: Minimum Required: * 3+ years of independent monitoring experience within the CRO or pharmaceutical industry * Independent monitoring experience in oncology clinical trials Other Required: * Availability for domestic travel, including overnight stays, which may constitute up to approximately 50–60% travel commitment; occasional international travel may be required * Fluency in Polish and English Preferred: * Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline * Experience monitoring complex early-phase oncology studies, including Phase I and/or CAR-T trials Why Precision for Medicine? Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology. Precision for Medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway. We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive changes for the company. 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/157136-cra-ii-scra.md) > Annual salary information is not provided for this position. 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