Sarah Jackson Email & Phone Number

United Kingdom

London, Gb

London, England, United Kingdom

Managed components of a complex global phase II cohort study protocol in bladder cancer as a member of the study team including EU country management of France, Germany, United Kingdom and Greece and vendor management of central lab (Labcorp) and protocol app vendor (Teckro). Involvement with many aspects of clinical trial management such as study start-up activities, including site selection and attending Site Initiation Visits (SIVs), Interim Monitoring Visit (IMV) report review, Informed Consent Form (ICF) review, protocol amendments, data and Important Protocol Deviation (IPD) oversight, Trial Master File (TMF) review (Veeva Vault), Clinical Trial Management System (CTMS) updates and Electronic Data Capture (Veeva EDC) / Interactive Response Technology (Endpoint) system oversight.

London, United Kingdom

Managed the STAMPEDE trial, a large oncology phase III study in prostate cancer with over 100 sites in the UK and Switzerland, covered many aspects of trial management and had a focus on pharmacovigilance (PV), ensuring that safety reporting processes were adhered to, including reporting to regulatory and ethics committees as required. Ensured all safety data was entered and reconciled in a timely manner for clinical safety committee review, data monitoring and data analysis deadlines. Submitted substantial protocol amendments for regulatory and ethics review and assisted in rolling out new protocol amendments to sites. Contributed to documentation updates including CRFs, the safety management plan, PV checklist and internal processing documents. Participated in site training and dealt with site queries, as well as being involved with central monitoring and dealing with protocol deviations. Gained line management experience managing one Data Manager.

London, Greater London, United Kingdom

Supported the Lead Project Manager with all project management activities across 10 global studies, including 2 large study programmes which varied in therapeutic areas and phases. Joined global sponsor meetings with clients based in the US, Europe and Asia and prepared the agendas and minutes, coordinated and oversaw study start-up and execution activities, monitored internal data flow, communicated with the sponsor regarding project status, prepared study metric reports and provided guidance and support to the operations team members. In the absence of the project manager, acted as the lead on the project and led project meetings with the sponsor team.

London, Greater London, United Kingdom

Carried out data management activities for 2 oncology trials, IoN and ORCA-2. Managed data entry from paper Case Report Forms (CRFs) into the Macro databases and raised queries as needed, processed pathology samples for central review, requested and processed central monitoring documents and communicated with sites.

Reading, United Kingdom

Provided administrative support to the running of Oncology and Haematology clinical trials, including document version control, database management and dealing with data queries and data entry.

Wrexham, Wrexham, United Kingdom

Crewe, United Kingdom

1st line IT support at Bentley Motors main site in Crewe. Auditing audio-visual equipment.

Reading, United Kingdom

Helping out showing prospective students around the biological sciences department at open days and visit days.

Reading, United Kingdom

6 week summer placement in haematology in the pathology department of Royal Berkshire Hospital. Tasks included following standard operating procedures to run blood samples on the automated machines to read full blood counts, erythrocyte sedimentation rates and coagulation tests as well as maintaining the machines and carrying out daily checklist duties in the laboratory.