Clinical Trial Manager Our client, a medical device organisation, are currently recruiting for a Clinical Trial Manager to join their team on a permanent basis.
As Clinical Trial Manager, you will oversee the execution of global clinical studies.
This role ensures clinical trials are delivered in compliance with regulatory and quality standards while meeting project timelines and business objectives.
The role is primarily remote with monthly visits to the Dublin office.
Responsibilities Lead the planning and execution of global clinical trials for medical devices Serve as project lead for one or more clinical studies, developing project plans, timelines, budgets, and resource requirements Coordinate cross-functional teams and external partners to ensure trials are delivered on time and within budget Oversee all phases of clinical studies including site activation, patient enrolment, follow-up, monitoring oversight, data management, and study close-out Ensure clinical activities comply with SOPs, Good Clinical Practice (GCP), and applicable regulatory requirements Develop and contribute to key clinical and regulatory documents (e.g., protocols, case report forms, study reports) Lead enrolment strategies and maintain communication with clinical sites and stakeholders Identify and manage risks, issues, and contingency plans throughout the trial lifecycle Manage relationships with clinical research organisations and external vendors.
Contribute to preparation of regulatory submissions and support clinical evidence generation for device approval Requirements Bachelors degree in science, engineering, or a related discipline 7+ years experience in medical device development or clinical research, including experience managing clinical trials Strong project management skills with experience planning timelines, resources, and budgets Knowledge of clinical trial regulations including FDA and Good Clinical Practice (GCP) Experience working with clinical research organisations and external partners Experience preparing clinical documentation for regulatory submissions Strong communication, organisational, and problem-solving skills For more information, please contact Sinéad Cullen on or