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.

Lead clinical trial operations for oncology and rare disease studies, ensuring compliance with protocol, SOPs and ICH-GCP. Responsibilities include site feasibility and start-up, CRA oversight and monitoring, eTMF and CTMS management, regulatory/IRB submissions, IP accountability, vendor management, training, and CAPA implementation. Position is remote in Australia and requires Mandarin proficiency and the ability to travel domestically and internationally.

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.

Precision for Medicine is hiring a Senior Feasibility Associate/Feasibility Manager to deliver evidence-based feasibility assessments across pre-award, post-award, rescue, and standalone engagements. Requires a bachelor's in life sciences or related field, at least 2 years relevant experience (feasibility, clinical operations, epidemiology, or similar), and professional proficiency in English. Role can be fully remote in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia; candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsible for conducting and presenting feasibility assessments (country, site, patient-pool, recruitment) across pre-award, post-award, rescue and standalone engagements; reviewing protocols and study assumptions; coordinating site/investigator outreach; collaborating with Business Development, Clinical Operations and other stakeholders. Requires a life-sciences bachelor's degree, professional English, and at least 2 years' relevant experience; knowledge of ICH-GCP and proficiency with Excel/PowerPoint/Word and web-based data platforms preferred.

Provides leadership and strategic direction for the Site Start-up (SSU) department, ensuring execution of SSU activities (e.g., informed consent adaptation, regulatory document collection and review, IRB/EC/CA submissions, and support for site contracts and budgets). Oversees large and complex SSU programs, drives process optimization and KPIs, partners with cross-functional teams, and supports team development and resourcing. Requires a minimum of 12 years in clinical research and fluency in English.

Responsible for end-to-end site start-up strategy and execution including ICF customization, IRB/EC and CA/MoH submissions, IMP release packaging, milestone planning and tracking, stakeholder coordination, translations, and mentoring staff. Requires a bachelor's degree or RN, 5+ years' start-up experience (CRO/pharma/biotech preferred), project milestone management experience, fluency in English and local language where applicable, and legal authorization to work without employer sponsorship.

Accountable for day-to-day clinical study operations as primary clinical contact with clients and internal teams. Responsibilities include site feasibility and start-up, monitoring strategy and execution, eTMF/CTMS management, IP accountability, vendor oversight, CAPA implementation, and supporting audits. Minimum 7 years clinical research experience; role based in the United States (remote) with domestic and international travel expected.

Lead development and oversight of investigator grant and site budgets during proposals and clinical trials, manage grant administration (payments, reconciliations, reporting) globally for LATAM countries, and collaborate with Project Directors/Managers. Requires ≥5 years clinical research experience, ≥3 years leadership experience, strong financial/analytical skills and fluency in English.

Responsible for ensuring timely, inspection-ready Trial Master Files across LATAM studies: create and execute TMF Plans and Indexes, manage document review and processing, perform/oversee periodic quality reviews, monitor TMF health/metrics, support audits and inspections, manage study close-out and eTMF handover. Requires a bachelor's degree (or equivalent), a minimum of 3 years related experience, professional working proficiency in English, experience with eTMF systems, and knowledge of ICH-GCP/FDA guidance.

Responsible for serving as the primary clinical lead for studies covering the China market, including site feasibility and start-up, CRA oversight, eTMF and CTMS management, regulatory/IRB submissions, IP accountability, metric reporting, and implementation of CAPAs. Requires coordinating with cross-functional teams, supporting investigator meetings, and ensuring data quality and compliance.