Loewenstein Kreger

Developed a Standard Operating Procedure (SOP) for the ICF review and approval process Submitted an abstract for the annual meeting of Society for Clinical Trials (SCT) Experience in Developing a Standard Operating Procedure for the ICF Review and Approval Process” .

Provide support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues Responsibilities.

Lead and Coordinates the research patient pathway from screening through to trial closure. Liaise with Clinical Trial Set Up staff to help assist in the set-up of trials on site. Lead and prepare for monitoring visits for site management and subject recruitment. Adopt a diligent and meticulous approach in order to produce and maintain complete and detailed records, in keeping with Good Clinical Practice.

Lead on effective communication and networking with Clinicians, surgeons and scientists in order to translate research needs into high participants recruitment and efficient sample collection and implement strategies to improve quality in clinical trials.

Research meetings as appropriate to discuss trial progress for the Investigators and Study Monitoring Team for both commercial and non- commercial trials and Lead and Coordinates the research patient pathway from screening through to trial closure.