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    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
    • Interest in healthcare IT and informatics.
    • Opportunity to shape a new and growing clinical informatics division.
    • Develop training materials and user guides.
    • You will work primarily in the office, with the flexibility to work remotely for 20% of your time (one day per week).
    • As the Clinical EMR Implementation Coordinator, your primary responsibility is to oversee the successful integration of an Electronic Medical Record (EMR)…
    • As a Data and Analytics Manager within our Health Practice, you will oversee the end‑to‑end lifecycle of health data, ensuring accuracy, compliance, and…
    • This role sits at the intersection of clinical domain expertise and cloud technology, requiring the ability to engage credibly with senior clinical and digital…
    • Experience in coding management, auditing, training, CDI or healthcare informatics is beneficial.
    • Shape AI-powered Clinical Coding solutions used across the NHS…
    • The issue of quality of data and information pervades all aspects of the delivery of patient care and is the responsibility of everyone involved in delivering…
    • Carry out centre visits to undertake sampling of assessment and internal verification decisions and records for competence/skills -based qualifications within…
    • The Sector Advisor (SA) will support the verification of the BTEC Level 2 Diploma in Healthcare Science.
    • Familiarise yourself with the specification so that you…
    • We are looking for an experienced digital programme or portfolio leader who combines strategic thinking with a practical delivery mindset, thrives in complex…
    • We're responsible for ensuring that Microsoft AI's models and services are useful, trusted and safe across diverse customer health journeys.
    • The informatics team utilises informatics principles and techniques to architect, mine, analyse, and visualise clinical trial data to inform study design…
    • Sitting at the intersection of capability building, innovation, and operational excellence, you will lead impactful learning and knowledge initiatives that…
    • Excellent understanding of clinical trials methodology, GCP and medical terminology.
    • This role is based in London, UK.

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Job Post Details

Senior Pharmacovigilance Officer - job post

Milpharm Ltd
Uxbridge UB11 1AF
£28,000 - £35,000 a year - Permanent, Full-time
Responded to 51-74% of applications in the past 30 days, typically within 3 days.

Job details

Pay

  • £28,000 - £35,000 a year

Job type

  • Permanent
  • Full-time

Location

Uxbridge UB11 1AF

Benefits

Pulled from the full job description

  • Sick pay
  • Life insurance
  • Company pension
  • Company events
  • On-site parking

Full job description

  • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
  • Assist in ensuring continuous oversight of all PV activities performed internally and by third parties.
  • Support regulatory inspections, audits, and CAPA management.
  • Contribute to PV governance activities and safety compliance monitoring.
  • Provide oversight of Medical Information activities to ensure compliance with pharmacovigilance obligations.
  • Ensure product complaints, adverse events, special situations, and safety information received through Medical Information are appropriately identified, processed, and reported.
  • Support and perform reconciliation activities between Medical Information and other stakeholders
  • Ensure deviation, CAPA, change control, and risk management processes.
  • Drive inspection readiness activities across the PV system.
  • Deliver pharmacovigilance training to internal stakeholders
  • Coordinate the preparation, review, and submission of PSURs, RMPs and ACOs in accordance with regulatory requirements.
  • Preparation and implementation and maintenance of approved RMM programmes.
  • Coordinate the preparation, review, UK PSMF and all associated annexes.
  • Ensure the PSMF accurately reflects the current pharmacovigilance system and organisational structure.
  • Oversight and management of safety variations

Qualification:

  • Essential Degree in Life Sciences, Pharmacy, Nursing, Medicine, or related healthcare discipline.
  • Significant pharmacovigilance experience within the pharmaceutical industry.
  • Strong knowledge of UK Pharmacovigilance legislation and MHRA GVP requirements.

Job Types: Permanent, Full-time

Pay: £28,000.00-£35,000.00 per year

Benefits:

  • Company events
  • Company pension
  • Life insurance
  • On-site parking
  • Sick pay

Ability to commute/relocate:

  • Uxbridge UB11 1AF: reliably commute or plan to relocate before starting work (required)

Education:

  • Bachelor's (required)

Licence/Certification:

  • UK Work Authorisation (required)

Work Location: In person

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