Associate Medical Director - London - ECS Resource Group

    ECS Resource Group
    ECS Resource Group London

    2 days ago

    Description

    Role OverviewThe Associate Medical Director will play a key role in providing medical leadership and clinical oversight across the full product lifecycle. This position works in close partnership with internal stakeholders to support clinical strategy, product development, regulatory submissions, and post-market activities.

    The role is inherently cross-functional, requiring collaboration with R&D, Quality, Regulatory Affairs, and Commercial teams, as well as engagement with external clinicians and Key Opinion Leaders to support evidence generation and medical strategy.

    Key Responsibilities

    Provide medical expertise and clinical guidance to product development activities, risk management, and customer-facing discussions

    Support the planning, conduct, and interpretation of clinical studies, including both pre-market and post-market investigations

    Act as medical monitor for clinical trials, reviewing safety data, evaluating adverse events, and ensuring appropriate patient protection

    Contribute medical input to post-market surveillance and complaint investigations

    Work closely with Regulatory Affairs and Quality teams to ensure compliance with applicable medical device regulations and clinical standards

    Build and maintain effective relationships with external clinical experts, investigators, and Key Opinion Leaders

    Support the creation and review of medical, scientific, and training materials

    Provide medical input to internal training initiatives and broader medical affairs strategies

    Skills & Experience

    MD, MBBS, or equivalent recognised medical degree (active medical registration preferred)

    At least 5 years of post-qualification clinical experience

    Demonstrated experience within the medical device industry, ideally in a medical affairs, clinical research, or medical monitoring capacity

    Strong understanding of clinical research processes, GCP, safety reporting, and medical device regulatory frameworks

    Proven ability to influence and collaborate within matrixed, cross-functional environments

    Excellent written and verbal communication skills, with the ability to explain complex medical concepts clearly

    Analytical mindset with strong clinical judgement and problem-solving capability

    Comfortable working in a dynamic, fast-paced environment

    Postgraduate qualifications in medicine, management, or a related discipline

    Prior experience supporting regulatory interactions or clinical submissions

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