The Role
We are seeking an experienced Medical Director (MD) or Senior Medical Director (SMD) to join our team in select EMEA locations. This is an exciting opportunity for an experienced medical monitor, ideally from another CRO, with a background as a Neurologist or Psychiatrist, to drive medical excellence across our clinical research projects.
As a Medical Director, you will be a trusted medical expert with specialized knowledge in your therapeutic area and experience across multiple indications, clients, and drug development phases. You will initiate and maintain strong medical and consultative relationships with clients, provide expert guidance on early engagement and pre-award opportunities, and serve as a medical monitor for contracted projects. Where appropriate, you may take on leadership roles by participating in strategic initiatives, mentoring junior physicians, and managing a team of medical professionals.
Key Accountabilities
Project Execution: Medical Monitoring Delivery & Pharmacovigilance Support
Independently deliver all medical support required for successful project delivery according to contracted agreements with sponsors, fulfilling all assigned tasks and timelines
Actively participate in study planning with feasibility leaders and solution consultants
Participate in team project meetings and investigator meetings
Provide training to study teams on therapeutic area indication and protocol (excluding direct medical advice on patient care or management)
Participate in the development and review of study documents including clinical protocols, Medical Monitoring Plans, integrated clinical and statistical summary reports, safety plans, and Informed Consent Forms
Deliver medical monitoring activities according to Medical Monitoring Plans during study conduct
Provide medical leadership to projects in close coordination with the Project Leader, serving as either Global Lead Physician or Regional Lead Physician as assigned
Provide medical input into pharmacovigilance workflows and participate in safety processing, including medical review of serious adverse events
Client Relationship Building & Engagement
Support business development efforts with medical expertise
Provide medical expertise to clients across multiple channels and interactions
Offer consultancy on protocol development and drug development programs
Conduct medical review of various documents that may be audited by clients and regulatory agencies
Required Qualifications & Experience
Medical qualification from an acknowledged medical school
Minimum 5+ years of clinical medicine and practice experience
Qualified Psychiatrist or Neurologist, with up to date knowledge and expertise
Experience as a medical monitor, ideally from another CRO
Background in clinical aspects of drug development, including medical monitoring and study design/execution
Knowledge of the drug development process including drug safety; experience in Pharmaceutical Medicine; experience leading, mentoring, and managing individuals or teams
Excellent English language skills (written and spoken)
What We Offer
Opportunity to work on diverse, innovative clinical research projects
Professional development and mentoring opportunities
Potential for leadership and team management roles
Competitive compensation and benefits package
Collaborative working environment with leading clinical research professionals
How to Apply
Interested candidates are encouraged to submit their CV and a covering letter outlining their relevant experience and interest in this role. Please note that this position is currently recruiting for an opening at the end of summer 2026.
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