Director, Global Clinical Development

Responsibilities

• Consult with stakeholders to optimize clinical trial designs and objectives
• Serve as a clinical consultant to cross-functional teams and regulatory agencies
• Author and oversee program strategies and clinical trials for drug safety and efficacy
• Interpret and communicate results for Phase I-IV investigations
• Act as a signatory on NDA submissions and clinical documentation
• Manage product life cycle innovations and enhancements
• Lead regulatory filing activities with strategic direction

Qualifications

• Clinician (M.D. or D.O.), preferably with a background in genetic, metabolic diseases, or immunology
• Qualified PhD or other doctorate holders may be considered with appropriate team support
• Supplementary degrees (e.g., Ph.D., M.P.H., M.B.A.) are advantageous
• Experience in pharmaceutical industry with 3-6 years in clinical research or drug development
• Thorough knowledge of clinical medicine, science management, and regulatory environments
• Strong communication skills with proficiency in Microsoft Office programs
• Demonstrated leadership and team management experience

Pay

$209,599 – $313,375 annually

Schedule

Remote - US based candidates only, no visa sponsorship available