Medical Manager

Key Responsibilities Clinical Program Delivery Support delivery of global clinical development programs Provide medical oversight to ensure study quality, timelines, and budget adherence Communicate program progress, risks, and updates to senior leadership Contribute to Clinical Affairs strategy and cross-functional alignment Support implementation of Quality by Design principles across studies Medical Monitoring & Clinical Development Provide medical monitoring across clinical trials Develop and maintain Medical Monitoring Plans Support protocol development and review Contribute to Case Report Form design and clinical documentation Review and interpret clinical and pharmacovigilance data Support preparation of Clinical Study Reports Site & Scientific Engagement Build relationships with investigators, physicians, and external experts Participate in investigator meetings and scientific discussions Act as the primary medical contact for study sites and project teams Provide scientific and technical leadership across programs Gather and communicate medical field intelligence Compliance & Pharmacovigilance Provide pharmacovigilance support for clinical and post-authorisation studies Ensure compliance with ICH GCP and applicable regulations Support audit readiness and regulatory inspections Maintain high standards of quality and clinical governance Operational Excellence Drive process improvements and operational efficiencies Support clinical trial modernisation and digital initiatives Assist with development of SOPs and clinical processes Contribute to strategic planning across the clinical portfolio Leadership & Representation Provide therapeutic area training to internal stakeholders Support scientific communications and external engagement Represent the organisation at scientific meetings and conferences Engage with health authorities when required Requirements MD (Doctor of Medicine) qualification required Minimum 3 years’ experience in a Medical Manager, Clinical Development, Clinical Research or similar physician-led role Experience in medical monitoring within clinical trials Strong knowledge of ICH GCP and international clinical research regulations Excellent communication and presentation skills Strong analytical, problem-solving and project management capabilities Ability to work independently and influence cross-functional teams Eligibility to work in the United Kingdom What’s on Offer High-impact physician role within a global specialty pharmaceutical company Direct involvement in innovative clinical development programs Opportunity to work alongside internationally recognised scientific experts Collaborative and entrepreneurial environment with strong visibility Competitive salary and benefits package Hybrid working model with three remote days per week