Precision for Medicine seeks a Senior Clinical Project Manager (Oncology) to lead end-to-end clinical trials (Ph I–IV) in a CRO setting. Responsibilities include full-service oversight across functional areas (data management, safety, clinical, medical monitoring, biostatistics), proposal and costing participation, client liaison, team coordination and ensuring study delivery to agreed scope, timelines and budget. Role requires at least 4 years of full-service project management experience in clinical trials and strong knowledge of GCP/ICH.

Partner with global pharmaceutical organisations to lead implementations of Veeva PromoMats/Vault or Salesforce.com, performing project management, solution architecture, and business/functional analysis. Requires 6+ years' implementation experience, fluent English, ability to travel (~20%), and legal right to work in Europe. Total compensation listed in HUF.

Responsible for developing patient-focused, risk-informed feasibility and operational strategies for clinical trial proposals. Collaborates with RFP teams and stakeholders to produce data-driven country, site and enrolment recommendations, prepare compelling proposal text and presentations, and support pre-award feasibility activities and innovative pilots. Requires strong clinical/CRO experience, analytical skills, stakeholder communication and leadership within assigned therapy areas.

Precision For Medicine is hiring a Start Up Specialist to prepare and submit clinical trial application dossiers, interact with Competent Authorities and Ethics Committees, maintain project plans/trackers and support site activation (including IMP release, essential documents, ICF customization and translations). Role requires fluency in Hungarian and English and experience in site start-up or regulatory/start-up roles within a CRO or pharma/biotech. Candidates located in Hungary, Poland, Serbia, Slovakia or Romania are eligible; employer will not sponsor work visas.

Precision for Medicine seeks a senior Clinical Trial Manager to lead clinical aspects of multi-country trials (site selection, start-up, monitoring, enrollment, data cleaning, close-out), mentor CRAs, ensure regulatory documentation and quality delivery. Role is remote (candidates in Hungary, Poland, Romania, Serbia or Slovakia), requires CRO/Pharma/Biotech clinical lead experience in oncology (including CAR-T and radiopharmaceuticals) and knowledge of ICH-GCP.

Precision for Medicine seeks a Clinical Trial Manager to lead clinical aspects of multi-country trials (site selection, start-up, monitoring, data cleaning, close-out), manage CRAs, ensure timelines and quality, and mentor team members. Role supports oncology and specialized modalities (CAR-T, radiopharmaceuticals); must be able to communicate in English and travel domestically and internationally. Candidates can work remotely in Hungary, Poland, Romania, Serbia or Slovakia.

Precision for Medicine is hiring a Clinical Trial Manager to manage clinical elements of oncology (including CAR-T and radiopharmaceutical) trials across multiple countries (Hungary, Poland, Romania, Serbia, Slovakia). Responsibilities include site selection, start-up, enrolment management, monitoring planning and execution, data cleaning, close-out, regulatory documentation, and leading CRAs. Requires a science/health-related degree, significant multi-country clinical trial management experience in CRO/Pharma/Biotech, knowledge of ICH-GCP, and effective English communication. Role requires availability for domestic and international travel.

Precision for Medicine seeks an experienced Clinical Trial Manager to lead clinical aspects of multi-country oncology trials (including CAR-T and radiopharmaceutical studies). Responsibilities include site selection and start-up, enrolment management, monitoring planning and execution, data cleaning, close-out, regulatory documentation, mentoring CRAs, and maintaining timelines and quality. Requires knowledge of ICH-GCP, relevant clinical trial systems (CTMS, eTMF, EDC, IXRS), effective English communication, and availability for domestic and international travel. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Precision for Medicine seeks an experienced Clinical Trial Manager to lead multi-country oncology (including CAR-T and radiopharmaceutical) trials for a precision medicine CRO. Responsibilities include site selection/start-up, monitoring, enrolment management, data cleaning, close-out, mentoring CRAs, and ensuring GCP/ICH-compliant delivery. Candidates must communicate effectively in English, be legally authorized to work without sponsorship, and be available for domestic and international travel.

Lead data manager for assigned clinical projects overseeing database development, UAT, edit checks, data entry quality, queries, medical coding, SAE/AE reconciliation, TMF documentation and vendor interactions. Requires experience with EDC systems, database migrations, SOPs, and prior Clinical Data Manager or Senior Clinical Data Manager experience (5+ years as CDM II or 8+ years as Sr. CDM). Oncology experience preferred.

Precision for Medicine seeks a Project Director to manage global or large oncology studies (portfolio-level responsibilities possible). Core duties include client liaison, project planning and execution, budget and financial oversight, risk/change management, quality and eTMF readiness, cross-functional team leadership, and support for bid defenses. Minimum qualifications include a degree in a science/health-related field (EU/NA) and at least 8 years of clinical research experience with a minimum of 5 years direct project management experience.

Project Director (remote) responsible for oversight of global or large oncology clinical trials or a portfolio of studies, acting as primary client liaison, managing budgets, project plans, risk/change management, quality and cross-functional teams. Position is offered fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Seeking an experienced Project Director to lead global or large oncology clinical trials and portfolios. Role is fully remote (candidates based in the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia) and involves client-facing leadership, project planning, budget and profitability oversight, risk and change management, quality/eTMF readiness, use of eTMF/EDC/CTMS and Microsoft Project, mentoring project managers, and occasional domestic/international travel. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Lead global or large oncology clinical trials and portfolios, oversee project managers and cross-functional teams, manage budgets, timelines, risk and quality (including eTMF inspection readiness and ICH-GCP compliance), and act as primary client liaison. Requires a minimum of 8 years in clinical research (at least 5 years direct project management), experience with eTMF/EDC/CTMS and Microsoft Project, and willingness to travel internationally.

Seeking an experienced Project Director to lead and oversee global or large oncology clinical trials (portfolio-level oversight possible). Responsibilities include client liaison, project planning, budget and profitability management, risk/change management, quality/eTMF readiness, cross-functional team leadership, and participation in proposals and bid defenses. Requires a minimum of 8 years in clinical research and at least 5 years of direct project management experience. Position is fully remote and offered from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia. Candidates must be authorized to work in the country of employment without employer sponsorship.

Seeking an experienced Project Director to oversee global or large oncology clinical studies and portfolios. Responsibilities include client liaison, project and financial management, quality and risk oversight (eTMF/ICH-GCP), mentoring project managers, supporting business development (bid defenses), and ensuring study execution across cross-functional teams. Position is fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia.

Hiring a Project Director to lead and oversee global or large oncology clinical studies or portfolios. Responsibilities include client liaison, project team leadership, budget and financial oversight, project planning, risk/change management, quality (eTMF) and regulatory compliance, mentoring project managers, and supporting bid defenses. Role is remote (UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia) and requires ability to travel; candidates must be authorized to work without employer sponsorship.

Responsible for end-to-end clinical project leadership (Project Leader / Senior Project Leader) including project planning, risk management, budget/P&L oversight, client relationship management, cross-functional team leadership and compliance with ICH GCP. Role supports Phase I–III trials and requires strong CRO experience, therapeutic area expertise (Oncology required; Ophthalmology, Neurology, Dermatology or Cardiovascular desirable) and strong written and spoken English. Fully remote (country stipulated) work available in listed locations.

Precision for Medicine seeks a Senior Feasibility Associate or Feasibility Manager (title depends on experience) to perform clinical-trial feasibility analyses across pre-award, post-award, rescue, and standalone engagements. The role involves protocol review, epidemiology and site analyses, recruitment forecasting, collaboration with cross-functional teams and clients, and contributing to feasibility methods and tools. Position can be fully remote in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.

Precision for Medicine is hiring a Feasibility Manager (or Senior Feasibility Associate depending on experience) to deliver country, site, patient-pool, and recruitment recommendations for pre-award, post-award, rescue, and standalone feasibility engagements. The role requires interpreting clinical and epidemiological data, performing site and landscape analyses, presenting findings to stakeholders and clients, and contributing to feasibility methods and tools. Requires a bachelor's in life sciences (or related), professional English, and a minimum of two years' relevant experience.