Medical Manager - Greater London - EPM Scientific

    EPM Scientific
    EPM Scientific Greater London

    2 days ago

    Description

    Overview


    I am currently hiring for an international specialty pharmaceutical organisation advancing innovative treatments. I am looking for a Medical Manager to provide scientific and medical leadership across clinical programs, ensuring high‑quality study design, execution and oversight.

    Key Responsibilities

    • Lead medical oversight for clinical studies, including protocol development and Quality‑by‑Design principles.
    • Act as medical monitor: safety review, medical queries, oversight of study conduct.
    • Support development of CRFs, Medical Monitoring Plans, and Clinical Study Reports.
    • Maintain strong relationships with investigators and clinical sites.
    • Provide medical input to pharmacovigilance activities for clinical and post‑authorisation studies.
    • Review clinical and safety data; identify risks and propose solutions.
    • Ensure inspection readiness and support GCP audits/inspections.
    • Contribute to process improvements, digital trial initiatives, and cross‑functional knowledge transfer.
    • Provide internal scientific training and represent the organisation at scientific meetings.
    • Support communication with regulatory authorities as required.

    Requirements

    • MD (or equivalent) from UK, EU, or USA.
    • 3+ years' experience in clinical research/clinical development.
    • Strong knowledge of ICH/GCP and global clinical trial regulations.
    • Experience in medical monitoring, protocol development, and clinical data review.
    • Excellent written and verbal communication skills.
    • Strong analytical, decision‑making, and project leadership abilities.
    • Ability to work independently, manage deadlines, and solve problems quickly.

    What You Get

    • Competitive salary and benefits.
    • Opportunity to impact patient care and contribute to meaningful scientific progress.
    • High exposure to senior scientific experts and strategic programs.
    • Collaborative, intellectually driven environment focused on clinical excellence.
    • Hybrid work model with two days on‑site.

    Desired Skills and Experience

    • Medical Doctor
    • Clinical Development
    • Clinical Trial Management
    • Medical Monitoring
    • Protocol Development
    • Quality by Design (QbD)
    • Pharmacovigilance
    • ICH/GCP Compliance
    • Clinical Data Review
    • Medical Affairs
    • Cross‑functional Leadership
    • Investigator Engagement
    • Clinical Site Management
    • Risk Management
    • Clinical Project Management
    • SOP Development
    • Scientific Communication
    • Regulatory Interaction
    • Inspection Readiness
    • Audit Support
    • Clinical Strategy
    • Medical Governance
    • Stakeholder Management
    • Scientific Writing
    • Problem Solving
    • Time Management

    If this aligns with your expertise and ambition, I invite you to take the next step and apply.


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