Senior Clinical Project Manager

DICE is a leading CRO with over 35 years of experience focused that serves biotech and big pharma companies in Europe and the US. In order to support our growth, we are looking to hire a Senior Clinical Project Manager. As a Senior Clinical Project Manager you will be the driving force behind the successful execution of clinical trials for our sponsor clients. You'll manage multiple studies across various therapeutic areas with a focus on oncology , ensuring delivery on time, within budget, and in full compliance with regulatory standards and the QMS system of DICE. This role demands strategic oversight, operational excellence, and client-facing and vendor facing finesse.ResponsibilitiesProject OversightLead the planning, initiation, execution, and closure of clinical trialsDevelop and manage project quotes, project timelines, budgets, and resource allocationEnsure adherence to protocol, GCP, regulatory requirements and the DICE QMS systemIdentify project risks and implement mitigation strategiesMonitor quality metrics and ensure continuous improvementVendor Coordination and operational oversightOversee selection and management of third-party vendors, including contracting, budgets and invoices.Operational oversight of clinical operations, regulatory and pharmacovigilance teams that are either contracted or collaborate on the projectsTeam LeadershipCoordinate cross-functional teams including, biostatistician, data managers, medical monitors and medical writersProvide guidance, mentorship, and performance feedback to project team membersClient & Stakeholder ManagementServe as the primary point of contact for sponsor clients throughout the study lifecycleBuild strong relationships and ensure client satisfaction through proactive communication and issue resolutionReporting & DocumentationMaintain accurate project documentation and ensure timely reporting to clients and internal leadershipPrepare study status reports, dashboards, and presentations Qualifications and skillsMaster's degree in Life Sciences, Nursing, Biomedical sciences, Pharmacy, or related field or similar through experience. Minimum 10 years of clinical research experience, with at least 5 years in a CRO project management roleProven track record managing Phase I–IV trials across multiple therapeutic areas. Experience in oncology is considered as a plus. Strong understanding of ICH-GCP, FDA, EMA, and other global regulatory guidelinesPMP or equivalent certification preferredExcellent communication, negotiation, and organizational skillsAttention to detail, ability to work independently and able to distinguish important points from detailsStress resistantProficiency in project management tools (e.g., MS Project, CTMS, eTMF systems)Our offerDICE is a clinical research organization (CRO), that supports clinical studies for pharmaceutical and biotechnology companies. We offer full service projects delivery to our sponsors, and have an internal team that is specialised in clinical data management, bio statistics, central imaging review, medical writing and medical monitoring. If you work with us then we can offer this package:A driver's seat position in clinical researchA young and dynamic work environment with close contact to our sponsorsPossibility to grow with and within our companyAn attractive salary with lots of extras, including a long term incentive plan based on company targets An easy to reach officePossibilities to work from homeA personal development path with tailored courses and trainingTake your career to the next level, and apply now. Email recruitment@dice-cro.com