Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London
Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology

Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London

London Full-Time No home office possible
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At a Glance

  • Tasks: Lead clinical development for innovative liver disease treatments and drive impactful research.
  • Company: Join GSK, a leader in transformative medicines with a collaborative culture.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in patients' lives through groundbreaking medical advancements.
  • Qualifications: Medical degree with experience in clinical research and drug development.
  • Other info: Work in a dynamic environment with strong career progression opportunities.

GSK is seeking a highly skilled Medical Director, Clinical Development, for an Advanced Pipeline Unit (APU) Hepatology group to provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on steatotic liver disease (SLD), including alcohol-associated liver disease (ALD). You will work with project teams to plan and ensure delivery of clinical research and development activities and establish efficient collaboration throughout all stages of development. You will report to the Senior Director/Clinical Development Lead for an asset in the SLD therapeutic area. This role is pivotal in driving GSK’s mission to deliver transformative medicines to patients, ensuring clinical excellence, regulatory compliance, and operational efficiency. The successful candidate will not only deliver results but also inspire and empower teams to achieve exceptional outcomes.

About RIIRU: The Respiratory, Immunology and Inflammation Research Unit (RIIRU) was formed in 2024 to identify and advance novel molecular targets with genetic associations to disease based on the foundational observation that targets with human genetic evidence supporting their causal role in the intended indication improves clinical success by two-fold. The remit of RIIRU is to identify novel targets based on human genetics, develop assets for clinical studies, and perform trials through to submission for approvals. This goal is enabled through strategic external (e.g., Flagship Pioneering, Vesalius, Muna Therapeutics and others) and GSK-internal partnerships (Research Technologies).

PLEASE NOTE: This career opportunity requires an on-site office presence (minimum of two days a week) at one of GSK’s US (PA or MA) or UK (Stevenage or London HQ) sites.

Key Responsibilities

  • Contribute to the clinical development strategy for a drug or program.
  • Ensure execution of clinical development plans (CDP) for product(s) and/or indication(s) and provide strategic oversight and management of clinical trials.
  • Lead clinical development activities from a therapeutic area and clinical trial perspective, including:
  • Provide clinical and medical oversight of ongoing clinical trials.
  • Lead clinical trials and asset-level activities in a matrix team structure.
  • Identify and highlight transformational opportunities where projects can offer highly significant benefit to patients.
  • Contribute to development of the Integrated Evidence Strategy (IES). Integrate scientific rationale, regulatory requirements, product development plans, and commercial goals to optimize asset indications and trials.
  • Contribute to clinical development discussions and teams at global regulatory interactions. Draft clinical components of global regulatory submissions/files (e.g., IND, NDA, BLA, MAA), including briefing documents, presentations, and responses to regulatory questions.
  • Promote innovative methodologies and processes including digital tools, encouraging others to think differently and adopt new ways of working.
  • Stay abreast of advancements in therapeutic area research, clinical trial methodologies, competitive environment, and regulatory space to maintain GSK’s competitive edge.
  • Basic Qualifications

    • Medical degree and clinical medical specialty training board qualification/registration in Internal Medicine or Primary Medical.
    • Experience in the global pharmaceutical/biotechnology industry.
    • Experience in clinical research and drug development.
    • Experience in medical monitoring activities and oversight.
    • Experience in leading regulatory submissions and managing global clinical trials.
    • Experience with ICH and GCP guidelines and regulatory requirements.
    • Matrix team experience within a clinical development setting.

    Preferred Qualifications

    • Medical degree and clinical medical specialty training board qualification/registration in Hepatology/Gastroenterology, Endocrinology or Nephrology.
    • Thorough understanding of SLD, including ALD and MASH, the underlying biology and potential therapeutic targets.
    • Experience in late-stage Hepatology drug development, including Phase 2 and Phase 3 clinical trial design, initiation, execution, and closure.
    • Solid understanding of needs and priorities of regulators, payers and prescribers in relevant global market(s).
    • Track record of building and maintaining strong relationships with internal and external stakeholders.
    • Demonstrated strong problem-solving skills and innovative thinking. Anticipate potential challenges, develop strategic approaches, and effectively communicate uncertainty to stakeholders while guiding teams through unclear circumstances.
    • Have an enterprise mindset by identifying opportunities for synergy across the organization.
    • Ability to use strategic thinking to analyze, interpret, and critically evaluate complex data and information. Anticipate obstacles and identify innovative solutions to ensure timely delivery of evidence that supports regulatory approvals and patient benefit.
    • Navigate ambiguity by anticipating regulatory challenges and proactively addressing issues.
    • Experience of clinical research methodology and principles of biostatistics to facilitate innovative and efficient designs of clinical trials and clinical development plans with clear data-driven decision rules.

    If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. If you are based in another US location, the annual base salary range is $202,500 to $337,500.

    Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London employer: Gsk

    GSK is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the field of clinical development. With a strong commitment to employee growth, GSK provides numerous opportunities for professional advancement and encourages a culture of inclusivity and empowerment. Located in vibrant areas such as Upper Providence, Boston, and London, employees benefit from a rich blend of professional and personal experiences, making it an ideal place for those seeking meaningful and rewarding careers in healthcare.
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    Contact Detail:

    Gsk Recruiting Team

    StudySmarter Expert Advice 🤫

    We think this is how you could land Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London

    ✨Tip Number 1

    Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.

    ✨Tip Number 2

    Prepare for interviews by researching the company and its culture. Understand their recent projects, especially in Hepatology, and think about how your experience aligns with their goals. We want you to walk in feeling confident and ready to impress!

    ✨Tip Number 3

    Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and get comfortable discussing your experience. We can’t stress enough how important it is to articulate your skills and achievements clearly.

    ✨Tip Number 4

    Don’t forget to follow up after interviews! A simple thank-you email can go a long way in showing your enthusiasm for the role. Plus, it keeps you on their radar. Remember, we’re all about making connections that last!

    We think you need these skills to ace Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London

    Clinical Development Strategy
    Clinical Trials Management
    Regulatory Submissions
    Medical Oversight
    Experience in Hepatology
    Knowledge of Steatotic Liver Disease (SLD)
    Innovative Methodologies
    Strategic Thinking
    Problem-Solving Skills
    Matrix Team Leadership
    Understanding of ICH and GCP Guidelines
    Clinical Research Methodology
    Biostatistics Principles
    Stakeholder Relationship Management
    Data Analysis and Interpretation

    Some tips for your application 🫡

    Tailor Your CV: Make sure your CV is tailored to the Medical Director role. Highlight your experience in clinical development, especially in Hepatology and related fields. We want to see how your background aligns with our mission at GSK!

    Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about hepatology and how you can contribute to our Advanced Pipeline Unit. Keep it engaging and relevant to the job description.

    Showcase Your Leadership Skills: As a Medical Director, you'll need to inspire and empower teams. In your application, share examples of how you've led projects or teams in the past. We love seeing candidates who can drive results and foster collaboration!

    Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at GSK!

    How to prepare for a job interview at Gsk

    ✨Know Your Stuff

    Make sure you brush up on the latest advancements in hepatology, especially around steatotic liver disease. Familiarise yourself with GSK's pipeline and how your expertise aligns with their goals. This will show that you're not just interested in the role but are genuinely invested in the company's mission.

    ✨Showcase Your Leadership Skills

    As a Medical Director, you'll need to inspire and empower teams. Prepare examples from your past experiences where you've successfully led clinical trials or managed cross-functional teams. Highlight how you navigated challenges and drove projects to success.

    ✨Understand Regulatory Nuances

    Since this role involves regulatory submissions, be ready to discuss your experience with ICH and GCP guidelines. Bring specific examples of how you've handled regulatory interactions or submissions in the past, as this will demonstrate your capability in managing compliance effectively.

    ✨Ask Insightful Questions

    Prepare thoughtful questions about GSK’s current projects, particularly in the Advanced Pipeline Unit. This not only shows your interest but also gives you a chance to assess if the company culture and goals align with your own values and career aspirations.

    Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London
    Gsk
    Location: London
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    • Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology in London

      London
      Full-Time
    • G

      Gsk

      10000+
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