Seeking a Project Director to manage global or large oncology clinical studies or a portfolio of studies. Duties include serving as primary client liaison, overseeing study planning/execution, managing budgets and profitability, implementing risk and change management, ensuring quality/eTMF readiness, mentoring project managers, and supporting bid defenses and proposals. Minimum qualifications include a degree in a science/health-related field (EU/NA) and at least 8 years in clinical research with a minimum of 5 years direct project management experience.

Fully remote Project Director for clinical trials (oncology) responsible for overseeing global or large studies and portfolios, leading cross-functional teams, managing budgets and profitability, ensuring quality (eTMF/inspection readiness), driving project planning, risk and change management, client engagement and bid defense activities. Requires minimum 8 years clinical research experience and significant project management experience.

Project Director role for clinical trials (focus on oncology) managing all aspects of global or large studies and portfolios, including budgeting, project planning, risk and change management, quality (eTMF) and client liaison. Requires a minimum of 8 years in clinical research and at least 5 years of direct project management experience. Position is fully remote and may require domestic and international travel; eligible remote locations listed as UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia.

Lead global or large clinical studies and/or a portfolio of studies as Project Director. Responsibilities include client liaison, overseeing project managers, full project lifecycle management (planning, execution, closing), budget and profitability oversight, risk and change management, quality and eTMF readiness, KPI reporting, and supporting business development. Requires minimum 8 years clinical research experience (and minimum 5 years direct project management), experience with eTMF/EDC/CTMS and strong knowledge of ICH-GCP. Role is remote and may be based in the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia; travel (domestic and international) is required.

Director-level role leading the Site Start-up (SSU) function to ensure delivery of SSU activities globally/regionally (Informed Consent review, regulatory/IRB/CA submissions, site contracts and budgets). Requires 12+ years in clinical research, expert knowledge of GCP/ICH, leadership experience, and fluency in English. Remote opportunities listed for Australia, China, Singapore, South Korea and Taiwan.

Senior consultancy role providing subject-matter expertise on companion diagnostic (CDx) and IVD regulatory strategy, global submission pathways (including FDA and EU IVDR), clinical trial assay use, analytical and clinical validation, quality system and lifecycle management. Requires substantial experience working with diagnostic manufacturers, pharmaceutical sponsors, and regulatory authorities; minimum ~7 years relevant industry/consulting experience.