Director, Clinical Development
$243.1k - $314.6kGilead
Responsibilities
- Provide medical monitoring for clinical trials including eligibility assessment, toxicity management, and safety surveillance
- Lead or contribute to protocol design, clinical study reports, and regulatory authority communications
- Coordinate data collection, analysis, and preparation of study reports and scientific presentations
- Guide cross-functional teams on clinical development deliverables and project timelines
- Present scientific findings at conferences and investigator meetings
Requirements
- MD with 4+ years clinical/drug development experience in biopharma, healthcare, consulting, or academia
- PharmD or PhD in clinical research/pharmacology with 6+ years scientific/drug development experience
- Experience in medical monitoring and managing clinical safety concerns
- Proven leadership of cross-functional teams in life sciences or healthcare environments
- Expertise in study protocol design, regulatory filings, clinical publications, and presentations
- Strong analytical abilities and project management skills for complex deliverables
- Thorough knowledge of pharmaceutical regulatory requirements and GCP standards
Compensation: $243,100–$314,600 base salary
Vacancy posted 5 days ago
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