Sarah Jackson

Sarah Jackson Email and Phone Number

Clinical Trial Manager and SASM for Amgen FSP @ ICON Strategic Solutions
London, GB
Sarah Jackson's Location
London, England, United Kingdom, United Kingdom
About Sarah Jackson

Driven clinical research professional with diverse experience spanning the pharmaceutical industry, academia, and the NHS, with a robust specialisation in oncology. Demonstrated expertise in conducting and managing clinical trials, data management, and regulatory compliance. Known for a detail-oriented approach and a commitment to advancing medical research and patient care. Passionate about leveraging knowledge and skills to contribute to groundbreaking developments in oncology. Looking to connect with industry leaders and explore opportunities for impactful collaborations.- Diverse clinical research experience in the pharmaceutical industry, academia, and the NHS- Strong specialisation in oncology, with a deep understanding of cancer treatment and research- Expertise in conducting and managing clinical trials, ensuring adherence to regulatory standards and protocols- Skilled in regulatory compliance, maintaining rigorous standards and ethical practices in research- Committed to patient care and medical advancements, consistently striving to improve outcomes and quality of life- Excellent communication and collaboration skills, fostering productive relationships with colleagues and stakeholders

Sarah Jackson's Current Company Details
ICON Strategic Solutions

Icon Strategic Solutions

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Clinical Trial Manager and SASM for Amgen FSP
London, GB
Employees:
7419
Sarah Jackson Work Experience Details
  • Icon Strategic Solutions
    Clinical Trial Manager And Sasm For Amgen Fsp
    Icon Strategic Solutions
    London, Gb
  • Gilead Sciences
    Senior Clinical Trials Management Associate (Oncology)
    Gilead Sciences Jul 2022 - Jun 2024
    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.
  • Ucl
    Clinical Trial Manager (Oncology)
    Ucl Jan 2020 - Jun 2022
    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.
  • Bioclinica
    Assistant Clinical Project Manager
    Bioclinica Dec 2018 - Jan 2020
    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.
  • Cancer Research Uk & Ucl Cancer Trials Centre
    Data Manager
    Cancer Research Uk & Ucl Cancer Trials Centre Sep 2017 - Nov 2018
    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.
  • Royal Berkshire Nhs Foundation Trust
    Research Assistant
    Royal Berkshire Nhs Foundation Trust Jan 2017 - Sep 2017
    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.
  • Wockhardt Ltd.
    Sterile Technician Class 100
    Wockhardt Ltd. Oct 2016 - Dec 2016
    Wrexham, Wrexham, United Kingdom
  • Mphasis
    It Service Desk
    Mphasis Aug 2016 - Oct 2016
    Crewe, United Kingdom
    1st line IT support at Bentley Motors main site in Crewe. Auditing audio-visual equipment.
  • University Of Reading
    Student Ambassador
    University Of Reading Jun 2013 - Sep 2015
    Reading, United Kingdom
    Helping out showing prospective students around the biological sciences department at open days and visit days.
  • Royal Berkshire Nhs Foundation Trust
    Medical Laboratory Assistant
    Royal Berkshire Nhs Foundation Trust Jul 2015 - Aug 2015
    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.

Sarah Jackson Education Details

Frequently Asked Questions about Sarah Jackson

What company does Sarah Jackson work for?

Sarah Jackson works for Icon Strategic Solutions

What is Sarah Jackson's role at the current company?

Sarah Jackson's current role is Clinical Trial Manager and SASM for Amgen FSP.

What schools did Sarah Jackson attend?

Sarah Jackson attended University Of Reading.

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