Manage assigned IT infrastructure projects from initiation to completion, including planning, budgeting/estimating, risk mitigation, stakeholder and vendor management, project reporting, and ensuring adherence to SLAs and safety/industry standards. Requires 3+ years of project experience and English (minimum B2); PMP or equivalent certification preferred.

Suvoda seeks an entry-level, analytically oriented Associate Project Manager to work on cross-functional teams delivering IRT solutions for randomization and drug supply management in clinical trials. Responsibilities include client liaison, requirements documentation and specification reviews, project schedule and scope management, UAT planning and support, training delivery, and post‑go‑live client support. A bachelor's degree is required; strong communication, organizational, analytical, and problem‑solving skills are emphasized.

Parexel seeks a Global Professional Engagement Coordinator / Senior Project Specialist (home-based in Poland or Romania) to finalize documentation, manage logistics and vendors, and ensure compliant scientific leader engagements under CSAs. Requires 3–5 years supporting medical affairs/KOL engagement, experience with Veeva Vault, contracting knowledge, strong English communication, and intermittent travel (10–20%).

Accountable for site start-up delivery including development of activation readiness strategy, IRB/EC and CA/MoH submission planning, ICF customization, IMP release package delivery, milestone planning and tracking, risk mitigation, contract/budget negotiation support, stakeholder communication, training/mentoring of staff, and producing country‑specific start‑up summaries. Position may be performed remotely from Serbia, Romania, Hungary, Slovakia or Poland. Minimum 5 years' start-up experience; occasional travel may be required.

The Start Up Lead is accountable for planning and executing site start-up activities (IRB/EC & CA/MoH submissions, ICF customization, IMP release, contract and budget oversight) across assigned countries, acting as SME and trainer, coordinating translations, maintaining milestone tracking, and supporting clients and cross-functional teams. Requires a bachelor's in life sciences or RN, 5+ years start-up experience (CRO/pharma/biotech), project milestone management experience, fluency in English, and knowledge of GCP/ICH. Position can be performed remotely from Serbia, Romania, Hungary, Slovakia, or Poland; occasional travel may be required.

The Start Up Lead will manage site start-up strategy and execution (including IRB/EC and CA/MoH submissions, ICF customization, IMP release), coordinate stakeholders and tracking systems, provide SME support and training, and mentor less-experienced staff. Requires a bachelor's in life sciences or RN (or equivalent) and at least 5 years' start-up experience; occasional travel may be required.

Responsible for execution of country site start-up strategy and planning (IRB/EC & CA/MoH submissions, ICF customization, IMP release packages), coordinating document collection and translations, tracking milestones and timelines, liaising with stakeholders and clients, training and mentoring staff, and acting as SME for country-specific start-up processes. Occasional travel may be required.

The Start Up Lead is accountable for executing site start-up strategy and planning, coordinating document collection and approvals, ICF customization, regulatory submissions (IRB/EC and CA/MoH), IMP release packages, milestone planning and risk mitigation. Requires a bachelor’s degree (or RN), minimum 5 years start-up experience (CRO/pharma/biotech), leadership in cross-functional activities, project milestone management experience, fluency in English and the local language of the country of placement, and occasional travel.

Seeking an experienced Project Director to oversee global or large oncology clinical studies or study portfolios. Responsibilities include client liaison, project and budget management, risk/change management, quality and eTMF oversight, leading cross-functional teams, and supporting proposals/bid defenses. Role is fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia and requires a minimum of 8 years' clinical research experience.

Project Director responsible for overseeing global or large oncology clinical trials or a portfolio of studies, serving as primary client liaison, managing project managers, budgets, profitability, project plans, risk/change management, quality (eTMF readiness), and stakeholder communications. Role is fully remote from specified countries and requires experience in oncology trials (RadioPharm experience desired), strong knowledge of ICH-GCP and SOPs, and proven leadership/mentoring abilities.

Remote Project Director role supporting global and large oncology studies or portfolios. Responsibilities include client liaison, oversight of project managers, budget and financial management, development and execution of project plans, quality and eTMF readiness, risk/change management, and mentoring. Minimum requirements include a degree in a science/health field (EU/NA criteria) and at least 8 years' clinical research experience with a minimum of 5 years' direct project management experience. Role requires ability to travel domestically and internationally.

Seeking an experienced Project Director to lead and oversee global or large oncology clinical studies or portfolios. Responsibilities include client liaison, project planning and execution, budget and financial oversight, risk and change management, quality and eTMF readiness, mentoring project managers, and supporting business development. Role is fully remote from specified European countries and requires travel as needed. Minimum 8 years clinical research experience and at least 5 years direct project management experience.

Lead and oversee global or large oncology clinical trials and portfolios, act as primary client liaison, manage project managers, budgets, profitability, quality (eTMF) and risk/change management, and prepare client and senior management reporting. Requires a minimum of 8 years' clinical research experience (and at least 5 years direct project management), proficiency with Microsoft Office, Microsoft Project, eTMF, EDC and CTMS, and availability to travel.

The Project Director will serve as primary client liaison and lead cross-functional teams and portfolios of global oncology studies. Key responsibilities include project planning and execution, budget and financial oversight, risk and change management, quality and inspection readiness (eTMF), stakeholder communication and presentations, mentoring project managers, and supporting business development. The role is remote (UK, Spain, Poland, Hungary, Romania, Serbia, Slovakia) and requires international travel.

Seeking an experienced Project Director to manage global or large oncology clinical trials or a portfolio of studies. Responsibilities include client liaison, study planning and execution, budget and financial oversight, risk and change management, quality and eTMF readiness, team leadership, and support of bid/proposal activities. Role is fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia. Minimum required experience includes substantial clinical research experience (stated minimum 8 years) and direct project management experience (stated minimum 5 years).

Lead and deliver global clinical trial projects for mid/large biopharma clients: develop and maintain project plans, manage risks, budgets/P&L, resources and client relationships, ensure quality and ICH/GCP compliance, and lead cross-functional teams. Strong CRO experience with Phase I–III knowledge, Oncology therapeutic expertise (required), other TAs desirable, and strong written/spoken English are required. Role is available as country-specified remote in the listed EMEA countries.

Responsible for developing project plans (scope, milestones, schedules, resources), tracking progress and changes, coordinating with development and QA, reporting status to stakeholders, identifying and mitigating risks to software releases, and maintaining project documentation. Requires a bachelor’s degree or equivalent, strong communication and organizational skills, and over 3 years managing software development projects.

Responsible for end-to-end project leadership of clinical trials (Phase I–III) for large pharma partnership clients: developing project plans, risk mitigation, budget and P&L ownership, client relationship management, and ensuring delivery to time, budget and quality in compliance with ICH GCP. Role is remote in specified EMEA countries and requires strong CRO clinical project management experience and fluency in English.

Payscale seeks an experienced Project Manager to lead implementations of its compensation management software across multiple geographies. Responsibilities include owning end-to-end project plans, tracking and reporting project MI, managing risks/issues/dependencies, driving mitigation and continuous improvement, and coordinating stakeholders across regions. The role operates in a remote-first model and may require occasional in-person events.

The Feasibility Manager/Senior Feasibility Associate conducts evidence-based feasibility assessments for global clinical trials, synthesizing protocol, epidemiology, site, and operational data to produce country, site, and enrollment recommendations. The role includes coordination with cross-functional teams, site outreach, presenting analyses to clients, and contributing to method and tool development.