Medical Director/Senior Medical Director - Neurology or Psychiatry - TALENT SEARCHVerified as a real position

Who we’re looking for

• 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 you’ll do

• 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

About the position

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Benefits

• 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