MCS Group is delighted to be partnering with our successful client, who is an innovative medical device company. They are seeking an experienced Clinical Research Manager to lead the planning, delivery, and oversight of clinical trials supporting regulatory submissions and product commercialisation. As the Clinical Research Manager, you will: Lead and coordinate clinical trial sites and investigators Manage study timelines, budgets, contracts, and vendors Prepare ethics submissions and regulatory documentation Ensure compliance with GCP, SOPs, and study protocols Deliver clinical trial data, KPIs, and performance metrics Support FDA and other regulatory submissions You will have: Degree in Life Sciences (or related discipline) Strong project management background Experience with clinical data analysis and medical device regulations Knowledge of GCP and QMS environments Excellent communication, organisation, and prioritisation skills You will get: Hybrid working Private Health care To speak in absolute confidence about this opportunity please send an up to date CV via the link provided or contact Kathy Donaghey Senior Specialist Consultant at MCS Group Even if this position is not right for you, we may have others that are. Please visit MCS Group to view a wide selection of our current jobs Not all agencies are the sameMCS Group are passionate about providing a first-class service to all our customers and have an independent review rating of 4.9 stars on Google Skills: Clinical Research Manager Research Manager Medical Device Research