23 Medical Director jobs in United Kingdom available for remote work from home. Apply for positions such as Medical Director, Medical Director, Medical Director, Medical Affairs - Neurology - Europe (Remote) and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Medical Director provides medical leadership and strategic direction for clinical development programs, ensuring study protocols meet scientific and regulatory standards. They serve as a Medical Monitor, interpret clinical trial data, and collaborate with multidisciplinary teams to drive successful program execution.
The Medical Director oversees the execution of clinical trials in Neuroimmunology, specifically focusing on Lupus SLE, for a top-5 pharma client. Responsibilities include developing clinical development plans, overseeing medical writing for protocols, and managing clinical teams and scientific risks.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The Medical Director will oversee Medicaid appeals, ensuring timely and consistent responses to member and provider disputes regarding medical necessity. They will provide clinical expertise to the grievance team and chair committee meetings to support effective health care resource utilization.
The Lead Director drives network strategy and performance improvement for medical drug reimbursement across hospital and provider partners. They design strategic initiatives, manage contract relationships, and ensure alignment with legal and regulatory frameworks.
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The Medical Director provides administrative oversight to medical staff, analyzes utilization data, and develops claim adjudication criteria. They also act as a liaison between the company and the medical community while researching new medical procedures and technologies.
The Medical Director provides administrative oversight to medical staff, analyzes utilization data, and develops claim adjudication criteria. They also act as a liaison between the company and the medical community while researching new medical procedures and policies.
The Medical Director will serve as the senior medical and scientific expert for uniQure in the UK, leading medical affairs strategy and launch-readiness activities. This role involves building relationships with key opinion leaders, managing the medical budget, and ensuring compliance with UK regulatory standards.
The Client Engagement Director leads strategic client relationships, ensuring financial health and high-quality execution of medical communications projects. They act as a primary point of contact, driving organic growth and aligning scientific strategy with brand objectives across cross-functional teams.
Support Medical Affairs leadership in developing medical and operational strategies while managing clinical trial activities. Lead direct reports and manage client relationships to ensure successful project delivery and patient safety.
Lead the integrated strategy for post-market clinical evidence, medical affairs, and government relations for AI-enabled medical imaging products. Drive product adoption and reimbursement through KOL engagement, policy advocacy, and the generation of robust clinical evidence.
Lead the strategic design and execution of early clinical development plans from first-in-human studies through clinical proof of concept. Collaborate with cross-functional teams to integrate translational science and biomarkers into regulatory filings and development decisions.
The Associate Medical Director is responsible for implementing global safety strategies and monitoring the safety profiles of investigational and marketed products. This includes generating safety deliverables, conducting signal detection, and managing risk management activities across the product lifecycle.
The Global Safety Physician is responsible for the global safety strategy and overall safety profile of investigational and marketed products throughout their lifecycle. This includes leading signal detection, benefit-risk evaluations, and the preparation of critical regulatory safety documents.
Leads medical safety activities, signal management, and risk management strategies for specific product franchises. Coordinates the production of aggregate safety reports and provides strategic safety input for global regulatory submissions.
Lead the global medical and evidence generation strategy for a lung cancer asset, coordinating with cross-functional teams to translate scientific insights into patient impact. Manage external partnerships with academic centers and clinical experts while providing leadership and mentoring to Global Medical Directors.
The Medical Director provides scientific input for core medical affairs activities, including strategy, HCP engagement, and evidence generation. They lead the Promotional Review Committee to ensure all materials are scientifically accurate and compliant.
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The Client Engagement Director is responsible for leading strategic client relationships and ensuring client satisfaction and organic growth. This role involves guiding project execution and maintaining financial health across assigned accounts.
This role involves managing direct reports, including coaching, training, and supporting staff development within the Medical Information Contact Center (MICC). The Associate Director will also ensure client success through oversight of assigned clients, managing deliverables, KPIs, and operational strategy.
This role involves managing direct reports, including coaching, training, and supporting staff development within the Medical Information Contact Center (MICC) team. The Associate Director will also ensure client success through oversight of assigned clients, managing deliverables, KPIs, and operational strategy.
The role involves providing medical expertise and oversight throughout the preparation, conduct, and reporting phases of clinical trials. Key duties include preparing high-quality protocols and performing ongoing reviews of medical data.
The Director is responsible for selling Medical Affairs Advisory and Medical Communications solutions to pharmaceutical and biotechnology clients to drive revenue growth. This involves identifying new business opportunities, managing the sales pipeline in Salesforce, and collaborating with internal teams to design high-impact client proposals.
The Study Physician provides medical expertise and oversight throughout the preparation, conduct, and reporting phases of clinical trials. Key duties include authoring high-quality protocols and managing trial risks and medical data reviews.
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