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.
Responsibilities
* 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
Qualifications
* 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
Benefits
* Hybrid working
* Private Health care
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