Thomas Bolger Email & Phone Number

Ireland

Ireland

Ireland

Ireland

London (2018-2019); Dublin (2019-2021)

London, United Kingdom

• Responsible for all aspects of Site Management and Monitoring of clinical studies from initiation through close out, remote monitoring, completion of visit reports and tracking in CTMS and other systems within.
• Involvement in Feasibilities and start up of studies assigned.
• Preparation of study documents and support in submissions.
• Assist in the preparation of study specific procedures and guidelines.
• Working with a local and international project teams.
• Perform source data verification of site data

London, United Kingdom

• Responsible for all aspects of Site Management and Monitoring of clinical studies from initiation through close out, remote monitoring, completion of visit reports and tracking in CTMS and other systems within.
• Involvement in Feasibilities and start up of studies assigned.
• Preparation of study documents and support in submissions.
• Assist in the preparation of study specific procedures and guidelines.
• Working with a local and international project teams.
• Perform source data verification of site data

London, United Kingdom

• Contact potential investigator sites in accordance with the project specific feasibility process to determine site interestAssure timely entry of feasibility results in Clinical Trial Management System (CTMS) and/or.
• Proactive contact of sites to discuss study progress
• Track subject enrollment status
• Track subject adherence to study visit schedule
• Resolve queries with sites
• Track drug/study supply inventory and process resupply

Sheffield, United Kingdom

Maintain, update, validate and clean clinical trial data to ICH-GCP standard. Review and resolve any issues that arise via Sponsor feedback.Generation of reports.Perform quality control of transfer data.Train new team members on study tasks.Coordinate a team of four people in completion of complex Data Management tasks.

Dublin

Maintain, update and clean clinical database to ICH-GCP standard. Maintain study documentation in preparation of internal/external audits.Perform QC audits of clinical database (Inform/Oracle/Fortis)Reconciliation of external vendor dataPoint of contact for vendors and clinical sites attempting to resolve data management issuesPrepare projects for.

Record temperature logs for freezers, fridges and incubatorsAliquot samplesRegistration of samplesHomogenise post mortem samplesGrow cell linesEnsure laboratory remained stocked at all timesSterilise and dispose of well platesPrepare various reagents and mediaCalibrate scalesClerical responsibilities

Responsible for acquiring primal and offal samples and testing for entero bacteria. Bacteria, e coli 0157 and total viable count. Ensuring lab remained fully supplied at all times.Preparing agar and nutrient brothPerform audits for hygiene

Pgcert Applied Statistics

B.Sc. (Hons.), Pharmaceutical Technology, 2.1