[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 Trial Manager AI Summary Precision for Medicine seeks an experienced Clinical Trial Manager to lead the clinical delivery of oncology studies across multiple countries. The role oversees site selection, start-up, enrollment, monitoring, data-cleaning, close-out, regulatory documentation, and CRA leadership. Success requires substantial oncology trial-management experience in a CRO, pharmaceutical, or biotech setting and strong command of ICH-GCP and clinical development processes. The manager will work remotely from Hungary, Poland, Romania, Serbia, or Slovakia while coordinating cross-functional teams, sponsors, and investigative sites. Experience with CAR-T therapies or radiopharmaceuticals is an advantage.[Apply for this job](#job-application)[View company](https://jobicy.com/company/precision-medicine-group.md)ShareRemote from[Romania](https://jobicy.com/job-region/romania.md), [Poland](https://jobicy.com/job-region/poland.md), [Hungary](https://jobicy.com/job-region/hungary.md)+2 more, [Slovakia](https://jobicy.com/job-region/slovakia.md), [Serbia](https://jobicy.com/job-region/serbia.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished8 Nov 2026Apply before8 Dec 2026Listing views76Application actions2Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. Opportunity details ## About this role. Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precision medicine CRO. 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, in addition to working across other therapeutic areas. You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don’t miss exploring working with us. About You: * You love having responsibility and a say in how clinical trials are run * You plan ahead, but have alternative options and a flexible approach * You are client focused * You are well organised and able to manage timelines and shifting priorities, without sacrificing quality. * You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly * You are a master at identifying any risks that threaten projects and handle them resolutely * You thrive and work with autonomy and ownership to deliver successful outcomes The day-to-day role, and how we will support your continued growth: * Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out * Successful execution of assigned trials and ensuring completion of trial deliverables * Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members * Mentoring and training of team members * Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor * Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities * Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction Qualifications: Minimum Required: * Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology Other Required: * Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated ‘clinical lead’ role). * Significant clinical trial management experience in the area of oncology * Experience with CAR-T and Radiopharmaceuticals would be a strong plus * Working knowledge of GCP/ICH guidelines and the clinical development process * Availability for domestic and international travel including overnight stays * Must be able to communicate effectively in the English language Skills: * Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS) * Demonstrated ability to develop positive working relationships with internal and external organizations * Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan Competencies: * Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement Precision 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. #LI-Remote #LI-TB1 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](https://jobicy.com/company/precision-medicine-group.md) 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/159676-clinical-trial-manager-3.md) > Annual salary information is not provided for this position. Explore salary ranges for similar roles in our [Salary Directory ›](https://jobicy.com/salaries.md) * ![Upload CV](data:image/svg+xml;base64,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) ### Upload your resume now To unlock remote work opportunities and be discovered by global employers. This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 5/5EasyHard ### Pace & Pressure 5/5RelaxedFast-paced ### Autonomy Level 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThis is a senior, high-accountability role managing complex multinational oncology trials, clinical quality, timelines, risks, and CRA performance. It requires deep regulatory knowledge and the ability to make sound operational decisions independently in a dynamic environment. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$110,000US market range (per year)$90k–$135k0$148.50k 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 and USD market estimate are inferred for an experienced Clinical Trial Manager in the US market; actual compensation will vary materially by eligible country, trial complexity, and oncology expertise. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial management](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20management.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)[CRO operations](https://jobicy.com/jobs?search_keywords=CRO%20operations.md)[Clinical monitoring](https://jobicy.com/jobs?search_keywords=Clinical%20monitoring.md)[CRA leadership](https://jobicy.com/jobs?search_keywords=CRA%20leadership.md)[Site selection](https://jobicy.com/jobs?search_keywords=Site%20selection.md)[Study start-up](https://jobicy.com/jobs?search_keywords=Study%20start-up.md)[Enrollment management](https://jobicy.com/jobs?search_keywords=Enrollment%20management.md)[Clinical data cleaning](https://jobicy.com/jobs?search_keywords=Clinical%20data%20cleaning.md)[Regulatory documentation](https://jobicy.com/jobs?search_keywords=Regulatory%20documentation.md)[Risk management](https://jobicy.com/jobs?search_keywords=Risk%20management.md)[CTMS](https://jobicy.com/jobs?search_keywords=CTMS.md)[eTMF](https://jobicy.com/jobs?search_keywords=eTMF.md)[EDC](https://jobicy.com/jobs?search_keywords=EDC.md) Sample interview questionsHow have you managed a multinational oncology study from start-up through close-out?I establish a detailed operational plan covering country activation, site readiness, enrollment, monitoring, data review, and close-out milestones. I maintain frequent risk reviews with CRAs and functional leads, use clear escalation routes, and adjust plans early when site performance or regulatory timelines change. What actions would you take if enrollment falls behind the study timeline? I would first review enrollment data by country and site to identify root causes, such as patient availability, competing studies, activation delays, or protocol burden. I would then develop targeted actions such as focused site engagement, feasibility reassessment, recruitment support, additional site activation, and transparent sponsor communication with measurable recovery milestones. How do you ensure CRAs provide consistent, high-quality site oversight? I set clear expectations through monitoring plans, SOPs, study-specific training, and routine review of monitoring reports and action items. I coach CRAs using quality trends and site feedback, address gaps promptly, and ensure critical issues are escalated and resolved within agreed timelines. Describe your approach to maintaining ICH-GCP compliance during operational delivery. I integrate compliance into routine oversight rather than treating it as a separate activity. This includes confirming site documentation, informed-consent processes, investigational-product accountability, safety reporting, monitoring findings, and timely CAPA follow-up, while collaborating closely with quality and regulatory colleagues. How do you communicate clinical risks to sponsors and internal stakeholders? I communicate risks early, factually, and with a proposed path forward. I summarize the impact on patients, quality, timelines, and budget where relevant, identify decision points and owners, and maintain an action log so stakeholders can track mitigation progress and remaining exposure. Next step ## Apply now. Follow the employer’s application method and review Jobicy’s safety guidance before sharing personal information. 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