47 Director Of Drug Safety jobs in the United Kingdom

Global Medical Director – Rare Disease

This position is to be based out of either Paris, France or London, UK.

As part of the Rare Diseases division, this Global Medical Director role will focus on a launch brand to treat Rare Liver Diseases. This is a very visible role with exposure to working with senior stakeholders and cross functional teams. This is a truly global role and a great opportunity for someone to expand on their global experience or step up from another International/Regional role.

For this role it is essential that any interested candidates have international Medical Affairs experience (preferably Global) and ideally worked in Hepatology or Rare Diseases.

Key responsibilities:

• Devise and execute global Medical Affairs launch strategy and plan
• Work closely with cross functional team on integrated plans
• Support the development of clinical & real-world evidence
• Plan and deliver advisory boards
• Develop and lead global congress and symposia activities
• Involvement in publication planning and speaker training programs
• Establish and nurture relationships with KOLs in scientific exchange
• Provide medical input into lifecycle management initiatives
• Attend all relevant major conferences

Candidate Requirements:

• Higher degree (preferably an MD) in the life sciences or relevant clinical discipline
• Therapy area experience in Hepatology, Gastroenterology, Rare Disease or the Specialty Medicine space is required
• Experience in an international Medical Affairs setting (preferably Global)
• Launch experience
• Strong leadership, stakeholder management and influencing skills

To apply for this position please use the “Apply” option or feel free to send your CV directly to the Pharma-Partners team via email

Global Medical Director – Rare Disease

This position is to be based out of either Paris, France or London, UK.

As part of the Rare Diseases division, this Global Medical Director role will focus on a launch brand to treat Rare Liver Diseases. This is a very visible role with exposure to working with senior stakeholders and cross functional teams. This is a truly global role and a great opportunity for someone to expand on their global experience or step up from another International/Regional role.

For this role it is essential that any interested candidates have international Medical Affairs experience (preferably Global) and ideally worked in Hepatology or Rare Diseases.

Key responsibilities:

• Devise and execute global Medical Affairs launch strategy and plan
• Work closely with cross functional team on integrated plans
• Support the development of clinical & real-world evidence
• Plan and deliver advisory boards
• Develop and lead global congress and symposia activities
• Involvement in publication planning and speaker training programs
• Establish and nurture relationships with KOLs in scientific exchange
• Provide medical input into lifecycle management initiatives
• Attend all relevant major conferences

Candidate Requirements:

• Higher degree (preferably an MD) in the life sciences or relevant clinical discipline
• Therapy area experience in Hepatology, Gastroenterology, Rare Disease or the Specialty Medicine space is required
• Experience in an international Medical Affairs setting (preferably Global)
• Launch experience
• Strong leadership, stakeholder management and influencing skills

To apply for this position please use the “Apply” option or feel free to send your CV directly to the Pharma-Partners team via email

Hobson Prior is seeking a Medical Affairs Manager to join a pharmaceutical organization in Hertfordshire. In this role, you will support the medical affairs team by managing operations, logistics, and medical advisors. You will also lead key projects and ensure the delivery of high-quality medical information and scientific services to both internal teams and external stakeholders. This position requires a collaborative approach, with a focus on compliance, process improvement, and cross-functional teamwork.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Oversee and track progress on medical programs to ensure timely execution of deliverables.
• Improve operational processes, provide guidance to team members, and resolve issues efficiently. Develop tools, templates, and reports to enhance team effectiveness.
• Support compliance commitments and manage key medical projects.
• Collaborate with the Head of Medical Affairs on operational activities such as vendor oversight, meeting coordination, metrics tracking, and product launch integration.
• Ensure the creation and submission of medical materials and support cross-functional initiatives.

Key Skills and Requirements:

• Background in clinical, scientific, or life sciences fields.
• Strong communication skills, both written and verbal, with the ability to engage effectively with senior management.
• Experience managing medical advisors and fostering teamwork in a collaborative environment.
• Knowledge of evidence-based medicine and its application in clinical practice.
• Familiarity with the ABPI Code of Practice and its practical implementation.
• Project management experience in cross-functional pharmaceutical projects.
• Understanding of local healthcare systems, patient pathways, and clinical pathway design.
• Business acumen and a proactive approach to identifying new opportunities.
• Experience in product launches and navigating barriers to optimal care.

For more information, please contact Calum Watson .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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• Role Expectation : Strong project management and Business Analysis, including planning, execution, and communication, excellent organizational and interpersonal skills, and the ability to work independently and as part of a team.
• Is familiar with/has worked with AI/Agentic AI projects.
• Stakeholder Management: Collaborating with medical experts, clinical research organizations (CROs), vendors, and internal teams.
• Project Planning and Execution: Developing project plans, defining objectives, and managing timelines and budgets.
• Regulatory Compliance: Ensuring all projects adhere to relevant regulations and guidelines (e.g., FDA, ICH).
• Data Management: Coordinating data collection, ensuring data quality, and data integrity
• Study Management: Overseeing clinical trials, NIS studies, and other research initiatives from start-up to database lock.
• Experience & Knowledge: Candidates should have about 10 years of experience in business consulting or project delivery, with significant exposure to the medical, life sciences, or pharmaceutical industry. They must demonstrate knowledge of regulatory processes, medical content, and compliance frameworks including GxP. Familiarity or experience in AI/Gen AI projects