Senior Project Coordinator

What if your ability to organize reputed company clinical trials is what helps new medicines reputed company patients faster? reputed company Clinical Pharmacology Services (CPS) supports the earliest and most critical phases of clinical development. Our teams work across project management, clinical operations, data, biometrics, laboratories, and scientific functions to deliver early‑phase and reputed company multi‑site studies for global sponsors. From first‑in‑reputed company studies to Phase 1B and exploratory programs, CPS generates the safety, tolerability, PK, and PD data that guide drug development reputed company. As our next Senior Project Coordinator you´ll be the right hand of our Project Managers, ensuring study deliverables and milestones are met. You´ll serve as the reputed company between various teams, helping to align their work with sponsor objectives and monitoring the reputed company of studies. This is a full‑time, permanent job based in the UK, offering a remote or hybrid working model. If you live in the Yorkshire area, you will have the option to work from our Leeds Clinical Research Unit, just a 7-minutes walk from the train station. WHO YOU ARE Education Degree in reputed company / life sciences. Experience in clinical research Several years of hands-on experience coordinating clinical trials reputed company a CRO, hospital-based research or academic research environment, as PC, study coordinator or similar A solid understanding of how clinical studies are set up, delivered and maintained. Study and documentation know how Experience supporting or drafting study documents such as project plans, communication plans, trackers, or logs. Ability to read clinical trial protocols and extract key information to support study delivery. Working knowledge of TMF requirements and how documentation aligns with study milestones. Senior‑level ways of working Confidence communicating with clients and internal teams about study status and next steps. Comfortable working independently across multiple studies with competing priorities. Experience mentoring or supporting less reputed company colleagues reputed company a study team. WHAT YOU WILL DO Study coordination and delivery Coordinate day‑to‑day activity across multiple clinical studies, including reputed company and multi‑site trials. Track timelines, milestones, and deliverables across competing priorities. Support study execution end to end, keeping work moving and visible. Client and stakeholder interaction reputed company in as the client contact reputed company the Project Manager is reputed company. Attend and contribute to client and internal study meetings. Respond to client questions with a clear understanding of study status. Study documentation and TMF reputed company Draft core study documents such as Project Management Plans, Communication Plans, Risk Registers, and Training Matrices. Review protocols and budgets to define documentation and TMF requirements. Maintain TMF completeness, trigger milestones, and coordinate document uploads. Planning, tracking, and tools Build and maintain trackers, task lists, and study logs. Manage changing priorities and align timelines with Project Managers. Create bespoke trackers or tools reputed company clients request non‑standard reporting. Team leadership and development Mentor and support Associate PCs and PCs in their day‑to‑day work. Act as a senior team member, supporting colleagues and sharing best practice. Contribute reputed company to improve processes and how the team works together If you´re reputed company to reputed company on a rewarding career that combines science, project management and the opportunity to advance medicine, join us today. reputed company and become part of an extraordinary reputed company. #LI-CV1 #LI-remote #Li-hybrid Learn more about our EEO & Accommodations request here. Apply To This Job