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Clinical Development Medical Director – Neuromuscular
Kerr DentalClinical Development Medical Director overseeing clinical development in Neuromuscular therapies at Novartis. Leading clinical strategy and execution to bring innovative therapies to patients.
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Gene TherapyCAR-Tclinical researchglobal drug developmentclinical trial methodologyregulatory requirementsgood clinical practicedata analysisclinical executionsafety monitoring
Soft Skills
leadershipcollaborationcommunicationinfluencestakeholder engagementcross-functional teamworkstrategic thinkingdecision-makingproblem-solvinginterpersonal skills
Certifications & Qualifications
Medical degree
Industry Keywords
clinical strategydevelopment lifecyclebenefit-risk assessmentNeuroscienceNeurodegenerationMovement disordersglobal initiativesadvisory boardsregulatory authoritieskey opinion leaders
About the role
Key responsibilities & impact- Lead the science that shapes the future of medicine
- Drive clinical strategy and deliver high-impact programs
- Partner with cross-functional leaders and external experts
- Translate scientific insight into clinical execution and influence regulatory strategy
- Guide critical decisions across the development lifecycle
- Engage with external stakeholders including regulatory authorities, key opinion leaders, and advisory boards
- Support benefit-risk assessment and safety monitoring in collaboration with patient safety teams
- Contribute to clinical strategy, standards development, and global initiatives across the development function
Requirements
What you’ll need- Medical degree required, with clinical training and medical specialization in either Neuromuscular or Neuroscience/Neurodegeneration and/or Movement disorders
- Expertise in Gene Therapy research especially CAR-T is highly desirable
- Several years of experience gained in clinical research or global drug development across early and late phases
- Proven experience leading or contributing to global clinical trials, including planning, execution, and reporting
- Strong knowledge of clinical trial methodology, regulatory requirements, and good clinical practice standards
- Demonstrated ability to analyse, interpret, and communicate complex scientific and clinical data
- Experience working effectively in global, cross-functional, and matrixed environments with diverse stakeholders
- Strong leadership, collaboration, and communication skills, with the ability to influence senior stakeholders.
Benefits
Comp & perks- Commitment to Diversity and Inclusion
- Flexible working hours
- Professional development opportunities