Louise Bell

Operations Director, UK Labs at Precision For Medicine
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Contact Information
us****@****om
(386) 825-5501
Location
Stevenage, England, United Kingdom, UK

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Experience

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Operations Director, UK Labs
      • Mar 2021 - Present

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Senior Manager, Project Coordination
      • Jun 2020 - Mar 2021

    • Project Coordination Manager
      • Jan 2019 - Mar 2021

    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Manager, Project Coordination
      • Oct 2018 - Jan 2019

    • Director of Laboratory Operations
      • Aug 2017 - Oct 2018

    • Laboratory Operations Manager
      • Apr 2017 - Aug 2017

    • United Kingdom
    • Biotechnology Research
    • 100 - 200 Employee
    • Laboratory Operations Manager
      • Sep 2014 - Apr 2017

      I am a successful and motivated scientist, project, operations and people manager with excellent communication, organisational and time management skills. I have worked in clinical trial operations for both an academic institution and a CRO for a number of years. Currently my main duties and responsibilities are focused on managing a large team of temporary laboratory technicians (zero hour contracts), as well as contract scientific staff and managers over multiple sites. I run operations… Show more I am a successful and motivated scientist, project, operations and people manager with excellent communication, organisational and time management skills. I have worked in clinical trial operations for both an academic institution and a CRO for a number of years. Currently my main duties and responsibilities are focused on managing a large team of temporary laboratory technicians (zero hour contracts), as well as contract scientific staff and managers over multiple sites. I run operations, targeting client satisfaction by preparing master and forecasting schedules, financial reviews and resource, recruitment, expansion and succession planning for the division. I conduct performance reviews annually and follow-ups where necessary. I am involved in process improvements, developing training packages, I am a GCP trainer and write and review SOPs. I manage a team holding samples under a HTA licence, write and review COSHH and risk assessments, and support communication with other divisions within the company. I have excellent records of client service, resource gap analysis, project management, group expansion and have taken part in a number of internal and external audits including those conducted by our QA division, the MHRA and HTA. I am comfortable multi-tasking and work well under pressure whilst being exposed to a variety of daily challenges. Show less I am a successful and motivated scientist, project, operations and people manager with excellent communication, organisational and time management skills. I have worked in clinical trial operations for both an academic institution and a CRO for a number of years. Currently my main duties and responsibilities are focused on managing a large team of temporary laboratory technicians (zero hour contracts), as well as contract scientific staff and managers over multiple sites. I run operations… Show more I am a successful and motivated scientist, project, operations and people manager with excellent communication, organisational and time management skills. I have worked in clinical trial operations for both an academic institution and a CRO for a number of years. Currently my main duties and responsibilities are focused on managing a large team of temporary laboratory technicians (zero hour contracts), as well as contract scientific staff and managers over multiple sites. I run operations, targeting client satisfaction by preparing master and forecasting schedules, financial reviews and resource, recruitment, expansion and succession planning for the division. I conduct performance reviews annually and follow-ups where necessary. I am involved in process improvements, developing training packages, I am a GCP trainer and write and review SOPs. I manage a team holding samples under a HTA licence, write and review COSHH and risk assessments, and support communication with other divisions within the company. I have excellent records of client service, resource gap analysis, project management, group expansion and have taken part in a number of internal and external audits including those conducted by our QA division, the MHRA and HTA. I am comfortable multi-tasking and work well under pressure whilst being exposed to a variety of daily challenges. Show less

    • United Kingdom
    • Biotechnology Research
    • 1 - 100 Employee
    • Translational Research Manager
      • Aug 2013 - Sep 2014

      I had direct management responsibility for the virology laboratory staff (up to 20 individuals) at our Cambridgeshire site. Responsibilities included; assigning translational study leads, research scientists and research assistants to study-specific tasks, coordinating laboratory time and equipment requirements across projects and maintaining a project and staff work schedule. I ensured staff compliance with GCP and GCP for laboratories, all relevant SOPs, company standards and policies and… Show more I had direct management responsibility for the virology laboratory staff (up to 20 individuals) at our Cambridgeshire site. Responsibilities included; assigning translational study leads, research scientists and research assistants to study-specific tasks, coordinating laboratory time and equipment requirements across projects and maintaining a project and staff work schedule. I ensured staff compliance with GCP and GCP for laboratories, all relevant SOPs, company standards and policies and prepared monthly metric reports for the Associate Director for Laboratory Services. I reviewed and reported internal resource requirements, identifed skill sets and experience for new staff, was involved in all aspects of recruitment, design and set up of training plans for new and existing staff, ensuring that competency sign off was secured prior to staff initiating specific tasks. I monitored staff workloads, ensured that staff performed their duties in accordance with their role and conducted annual performance reviews. I was also involved in a number of special projects, such as scheduling software design, HTA licence compliance and SOP review. I regularly used to split my time between four of the six Retroscreen sites delivering staff training, in Ely, London, Manchester and Bourn. Show less I had direct management responsibility for the virology laboratory staff (up to 20 individuals) at our Cambridgeshire site. Responsibilities included; assigning translational study leads, research scientists and research assistants to study-specific tasks, coordinating laboratory time and equipment requirements across projects and maintaining a project and staff work schedule. I ensured staff compliance with GCP and GCP for laboratories, all relevant SOPs, company standards and policies and… Show more I had direct management responsibility for the virology laboratory staff (up to 20 individuals) at our Cambridgeshire site. Responsibilities included; assigning translational study leads, research scientists and research assistants to study-specific tasks, coordinating laboratory time and equipment requirements across projects and maintaining a project and staff work schedule. I ensured staff compliance with GCP and GCP for laboratories, all relevant SOPs, company standards and policies and prepared monthly metric reports for the Associate Director for Laboratory Services. I reviewed and reported internal resource requirements, identifed skill sets and experience for new staff, was involved in all aspects of recruitment, design and set up of training plans for new and existing staff, ensuring that competency sign off was secured prior to staff initiating specific tasks. I monitored staff workloads, ensured that staff performed their duties in accordance with their role and conducted annual performance reviews. I was also involved in a number of special projects, such as scheduling software design, HTA licence compliance and SOP review. I regularly used to split my time between four of the six Retroscreen sites delivering staff training, in Ely, London, Manchester and Bourn. Show less

    • United Kingdom
    • Research Services
    • 700 & Above Employee
    • Senior Research Associate (Research Manager)
      • Jun 2012 - Jul 2013

      This role involved the coordination and management of the day-to-day running of a busy research laboratory. This included taking the lead on special projects, managing procurement processes to a budget of up to £500,000 per annum, ensuring the health and safety of staff, arranging for research projects to be conducted according to EU and UK statutory requirements and aiding in the design and development of these projects.

    • Research Associate
      • Nov 2006 - Jun 2012

    • United Kingdom
    • Research Services
    • 700 & Above Employee
    • Research Assistant
      • 2001 - 2002

    • United Kingdom
    • Research Services
    • 700 & Above Employee
    • Research Assistant
      • 2000 - 2001

    • Senior Research Technician
      • 1996 - 2000

Education

  • University of Cambridge
    PhD, Molecular Virology
    2002 - 2006
  • Anglia Ruskin University
    Bachelor of Science (BSc), Cell/Cellular and Molecular Biology
    1997 - 2000

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