We are redirecting you to the source. If you are not redirected in 3 seconds, please click here.

Project Data Manager - Europe at Allucent. Lead clinical data. Partner with sponsors. Deliver quality trials.. We are looking for a . Project Data Manager (PDM). to join our Data Management A-team at Allucent. As a Project Data Manager, you are responsible for leading and coordinating end-to-end data management activities across clinical trials and biometrics stand-alone projects, ensuring high-quality, compliant, and timely delivery of clinical data.. At Allucent™, we are dedicated to helping small and mid-sized biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.. The role. You will  lead and oversee data management activities, timelines and finances of the Allucent Data Management (DM) department.  . Manage and coordinate DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meet the quality standards and regulatory requirements for analysis and reporting.    . You are responsible for the overall coordination and management of Data Management/Biostats standalone projects, large and complex trials and/or multiple projects belonging to one client.  . You work closely with sponsors, vendors, and internal teams to ensure data is collected, cleaned, reviewed, and delivered to the highest standards. You combine hands-on clinical data management expertise with strong project leadership, keeping timelines, scope, quality, and budgets on track.. Your main responsibilities will be:. Lead and oversee Data Management activities from database design through to database lock. Act as the primary point of contact for Data Management for sponsors, vendors, and internal stakeholders. Plan, coordinate, and deliver biometrics and clinical data projects according to scope, timelines, and contract. Establish and maintain clear communication, escalation, and risk management plans. Lead internal and external meetings, including Kick-Off Meetings and sponsor discussions. Manage vendors and support vendor selection and oversight where required. Oversee project budgets, financial health, and monthly status reporting. Supervise and support junior Data Management team members, ensuring quality and development. You are an experienced clinical data management professional who enjoys taking ownership, working closely with clients, and bringing structure to complex studies. . You will bring the following skills and experience: . Life science, healthcare degree and/or combination of education and experience . Minimum 8 years of relevant work experience in Clinical Data Management or related experience within Biometrics  . Minimum 8 years of relevant experience in related clinical trials environment . Thorough knowledge and understanding of ICH-GCP, 21CFR11 data privacy (GDPR/HIPPA) guidelines and awareness of local/regional requirements . Experience as DM Lead on several studies and experience in covering all phases of a clinical study (start up, conduct and database lock). Worked on multiple indications and clinical phases (I-IV) . Thorough understanding of EDC (Medidata or Veeva) database components and experience in technical data management practices (validation plans, testing, and documentation . Experienced in CDISC conventions, i.e., CDASH, TAUG models and hands on experience implementing these models . Confidence working directly with sponsors and external vendors. A collaborative mindset and the ability to mentor and guide others. Strong communication skills in English and comfort working in a global environment. Company Location: Ireland.