Provide clinical oversight and input into trial documents and strategic development plans
Contribute to regulatory documents including safety updates and submission dossiers
Act as medical monitor, ensuring safety and scientific integrity of clinical trials
Review clinical trial data and support final analysis and reporting
Support benefit-risk assessments and contribute to safety management activities
Mentor and coach clinical development team members to foster growth and collaboration
Deliver medical/scientific training and represent the franchise in internal sessions
Lead clinical trials as Clinical Scientific Lead, guiding all medical aspects
Requirements
Medical degree (MD or equivalent) with clinical training in internal medicine or a relevant sub-specialty
Minimum 3 years of experience in clinical research or drug development across Phases I–IV
At least 2 years of experience conducting global clinical trials in a pharmaceutical setting
Proven ability to interpret and present clinical efficacy and safety data
Strong understanding of GCP, clinical trial design, statistics, and regulatory processes
Excellent communication, interpersonal, and stakeholder engagement skills
Fluent in written and spoken English.
Benefits
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical oversightregulatory documentsclinical trial data analysisbenefit-risk assessmentsclinical trial designGCPstatisticsdrug developmentclinical efficacy data interpretationsafety data interpretation