Director, Clinical Trial Operations EMEA

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: We’re looking for a Director, Clinical Trial Operations EMEA on the Clinical Operations - Trial Operations team to help us expand what’s possible for patients with serious diseases. Reporting to the Sr. Director, Clinical Trial Operations, EMEA / APAC, you’ll be accountable for providing the leadership, strategic, operational planning and oversight of 1-2 indications within one compound to ensure all are delivered on time, within budget and with high quality. This role may manage clinical operations team members, as delegated by supervisor, to ensure the effective and efficient execution of all operational aspects of clinical study planning, implementation, data delivery and reporting. Selected candidate will represent Clinical Operations in a range of cross-functional groups, global functional committee(s) and initiatives intended to enhance function and company efficiency and productivity, regionally, and globally. This is a remote role and can be located in the United Kingdom or in Switzerland. What You'll Do: In this role, you’ll have the opportunity to be the primary operational lead over an 1-2 indications within one compound, in collaboration with the Senior Director, Clinical Operations. Ensures consistent and successful execution of operational aspects of regional and global studies as appropriate, including timelines, budget, data delivery and reporting, vendor management, GCP, etc. You’ll also: Develop operational strategies for implementation of clinical studies regionally/globally in conjunction with project teams and other cross functional departments. Ensure a “Quality Mindset” is in place across the organization by focusing on detailed plans to monitor the conduct of our studies, the management of our vendors and working closely with our QA organization to implement and manage a process for Inspection Readiness. Contribute to the development and review of regional/global policies and procedures. Ensure compliance with all Company/Regulatory requirements & TMF quality standards. Work with outsourcing/procurement management to optimize the vendor governance structure, incorporate performance metrics, and contribute to outsourcing discussions. Provide leadership to Clinical Operations staff and to project teams for vendor evaluation, selection, management and quality-based oversight. Assume responsibility for the management and leadership of the operations staff within the Clinical Operations group including recruitment, training, mentoring, career development, work assignments, performance evaluations and ongoing feedback to and of staff. Benchmark, track and report operational and study metrics with the ability to digest complicated or complex issues and communicate program statuses in a concise fashion to an executive audience with the ability to identify critical path items and mitigation plans. Have oversight of compound budget with the ability to manage variance to a minimal threshold. Ability to manage the accrual process as well as provide budget forecasting and scenario planning based on multiple study designs. Posses ability to represent Clinical Operations in a professional manner to executive audiences including attendance at requested meetings (i.e., Global Clinical Team, Global Project Team, etc.) Who You Are: You have a B ... (truncated, view full listing at source)