Bridget King

Bridget King Email and Phone Number

Pharmacovigilance Consultant - Risk Management @ Sagittal Pharma Consulting Ltd
Leatherhead, GB
Bridget King's Location
Leatherhead, England, United Kingdom, United Kingdom
Bridget King's Contact Details

Bridget King personal email

n/a
About Bridget King

Pharmacovigilance and risk management professional with significant expertise as a consultant and as a regulator. Over 7 years' experience as a senior pharmacovigilance consultant providing strategic advice on risk management, safety and legal status switch applications both pre- and post-approval for a wide range of medicinal products. Supported multiple Project Orbis submissions including EU and Core RMPs and associated Australian and Canadian annexes. Prior to this, 13 years' experience as a regulator at the UK's MHRA including monitoring safety of medicinal products, risk management and minimisation, and assessment of benefit/risk to protect public health at both European and National levels. Background includes Clinical Biochemistry (PhD), Biotechnology (BSc), and Post Graduate Certificates in Pharmacovigilance and Pharmacoepidemiology and in Epidemiology Evaluation of Vaccines.

Bridget King's Current Company Details
Sagittal Pharma Consulting Ltd

Sagittal Pharma Consulting Ltd

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Pharmacovigilance Consultant - Risk Management
Leatherhead, GB
Employees:
7
Bridget King Work Experience Details
  • Sagittal Pharma Consulting Ltd
    Pharmacovigilance Consultant - Risk Management
    Sagittal Pharma Consulting Ltd
    Leatherhead, Gb
  • Bjk Pharma Consulting Ltd.
    Director And Pharmacovigilance Consultant
    Bjk Pharma Consulting Ltd. Sep 2019 - Present
  • Ipsen
    Gps Senior Scientist
    Ipsen Mar 2020 - Jun 2021
  • Nda Group Ab
    Senior Consultant Contract
    Nda Group Ab Jan 2014 - Sep 2019
    Pharmacovigilance & Drug SafetyPharmacovigilance and risk management expertise as a senior consultant supporting clients with marketing authorisation applications (MAAs) for a wide range of products - experience providing strategic advice, drafting and reviewing Risk Management Plans (RMPs), briefing documents, MAA procedural responses and presenting at regulatory authority scientific advice meetings.
  • Medicines And Healthcare Products Regulatory Agency (Mhra)
    Senior Pharmacovigilance Assessor
    Medicines And Healthcare Products Regulatory Agency (Mhra) 2000 - Dec 2013
    London, United Kingdom
    Thirteen years pharmacovigilance experience monitoring a portfolio of medicinal products to ensure benefits outweigh risks at the MHRA with my most recent position as an Expert Scientific Assessor in the Vaccines, Anti-infectives and Advanced Therapies Unit within the Division of Vigilance and Risk Management of Medicines.Responsible for monitoring the safety of medicinal products and protecting public health by taking measures to minimise risks to patients through appropriate regulatory action and targeted communications. Experience in regulatory processes and benefit/risk assessments. Portfolio of medicinal products includes vaccines, genito-urinary medicines, dialysis solutions, obesity products, contrast agents, ophthalmic products, biosimilars and oncology medicines.

Bridget King Skills

Pharmacovigilance Regulatory Submissions Vaccines Regulatory Affairs Public Health Regulatory Requirements Biotechnology Medicine Drug Safety Mhra Healthcare Prescription Drugs Risk Management Plans

Bridget King Education Details

Frequently Asked Questions about Bridget King

What company does Bridget King work for?

Bridget King works for Sagittal Pharma Consulting Ltd

What is Bridget King's role at the current company?

Bridget King's current role is Pharmacovigilance Consultant - Risk Management.

What is Bridget King's email address?

Bridget King's email address is br****@****.gov.uk

What schools did Bridget King attend?

Bridget King attended University Of Cambridge, National University Of Ireland, Galway.

What skills is Bridget King known for?

Bridget King has skills like Pharmacovigilance, Regulatory Submissions, Vaccines, Regulatory Affairs, Public Health, Regulatory Requirements, Biotechnology, Medicine, Drug Safety, Mhra, Healthcare, Prescription Drugs.

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