Perry Smith Email & Phone Number

Hatfield, England, United Kingdom

Regional clinical operations lead for phase II study.Global clinical operations lead for Extended Access Programs, and post marketing studyResponsibilities include:-Efficient relation building with study CRO-Review of study data (missing pages, queries, SDV)-eCRF and IRT access management-Site close out management -IMV report reviews-Ethics package review-ICF and patient facing material review-Vendor management-IRT user requirement specification review (URS), and user acceptance testing (UAT)-Invoice approvals

Hatfield, England, United Kingdom

Support the epilepsy team by accurately maintaining clinical systems and trackers in line with project timelines. My main responsibility was to ensure eTMFs (NA, EMEA, APAC and Japan) were audit ready at all times. Other responsibilities included tracking of invoices, EDC and IRT system access management, distribution of safety update reports, lab kit management, review of site activation packages, and other day to day activities with the CRO and internal team.

Sydney, Australia

Clinical unit support by producing and maintaining study documentation, data collection (clinical procedures/assessments including IP administration), and data handling (data entry/query resolution) in phase I healthy volunteer and phase II oncology patient research. The role also involved hosting CRAs for SDV.

Uxbridge, Greater London, United Kingdom

As a CMA I was the main point of contact between PAREXEL and sites conducting phase II-IV clinical drug research. Excellent communication, time management and Microsoft package skills were essential. My responsibilities included:-Conduct and facilitate study specific start up activities -Manage site research activities-Review of site data-Invoicing-Document filing

The CPC role mainly consisted of being a point of contact between clients and departments working closely with project management. I co-ordinated sponsor visits and would also oversee data collection and database entry for phase I clinical research. Time management, organisation and leadership were key requirements of this job. My responsibilities included:-Assist in development of ICFs, Lab Manuals and protocol training slides-Set up of sub contractors-Day 1 Monitoring-Host CRAs-Generation of CRF paperwork-Assist Project Managers with close out activities-Manage data queries-Data entry

Assisting in the production and formatting of phase I study documents including CRFs and study worksheets as well other tasks such as:-Dispatch documents to clients-ICF/Protocol release and recall-Maintenance of delegation logs-Set up clinical study folders-Archiving of study documents-Data entry

Nottingham, United Kingdom

Perform clinical procedures and record data accurately in CRFs in accordance with ICH-GCP. Excellent organisation, interpersonal skills and team work was needed for work with stringent timelines under high pressure. My responsibilities included:-Gamma scintigraphic imaging-Venipuncture and cannulation-Perform 12 lead ECG-Record vital signs-Perform spirometry-Sample Processing (Laboratory work)-Immediate Life Support trained

Nottingham, United Kingdom

A module tutor for 20 Sport and Exercise Coaching 1st year students at Nottingham Trent University focusing on statistical analysis using the software SPSS.

Level 2 Diploma, Electrical Installations (Building And Structures)

Modules Include: Principles of Electrical Science Electrical Installation Technology Installation of Wiring Systems and Enclosures.

Master'S Degree, Sport Science, Distinction

Areas of research included bone metabolic response to exercise, beta-alanine and sodium bicarbonate supplementation on rowing performance.

Bachelor Of Science (Bsc), Sport And Exercise Science, 1St

Areas of study include sport physiology, environmental physiology, nutrition, psychology, observation analysis, biomechanics, exercise.