United Kingdom
My current roles and responsibilities include support and assisting in CE marking for new product and claim extension of existing product. Role includes creating clinical evaluation plan, review of literature and the writing of a Clinical evaluation report to Med Dev 2.7.1 Rev 4(2016) to assist in regulatory submission. I also manage the clinical programme of clinical trials pre CE mark , PMCF and case studies. This includes the writing of clinical plan, protocols, CRF, and ICF. and managing financial and legal agreements . I play and active part in project teams for NPD and monitor the lifecycle of existing devices through managing post market surveillance.
Managed a team of clinical support nurses who are instrumental in delivering education and training to the NHS in regards to wound care / dressing selection. Since April 2013 managed the Surgical clinical support nurses as well in delivering a valued added service to customers within a surgical environment. Have written and developed the educational material provided by AMS.
Responsble for the sales of wound care and single use instruments into the North West NHS trusts.
Sold both Hartmanns Wound care and Continence range of products. Was consistent in meeting all targets set. Assisted with induction / training of new sales executives.
Managed a ward of 28 beds on a day to day basis. Tissue viability link nurse Prioritised patients to ensure they had the best clinical outcome.