Senior Director Clinical Development, Solid Tumor
New
J
JobgetherOncology Clinical Development
Remote work opportunity within the United States.Full-TimeDirector
SalaryBase salary range of $299,800–$369,800 per year
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Job Details
- Languages
- English
- Experience
- At least 6 years of clinical development experience, including 5 or more years focused on oncology; 10+ years of relevant experience is preferred.
- Required Skills
- LeadershipProject Management
Requirements
- MD, DO, or equivalent medical degree in a relevant discipline.
- At least 6 years of clinical development experience, including 5 or more years focused on oncology; 10+ years of relevant experience is preferred.
- Deep professional knowledge of oncology therapeutics, with strong understanding of solid tumors and immuno-oncology.
- Demonstrated experience developing and executing clinical development strategies and plans across global programs.
- Strong understanding of international clinical development regulations, compliance requirements, and health authority expectations.
- Proven ability to analyze and interpret clinical data and translate scientific findings into development strategy and business recommendations.
- Experience developing clinical and regulatory documentation, including protocols, clinical study reports, and regulatory submissions.
- Demonstrated ability to build productive relationships with investigators, key opinion leaders, and advisory boards.
- Strategic leadership experience, including the ability to build, manage, mentor, and develop high-performing clinical development teams.
- Excellent written and verbal English communication skills.
- Willingness and ability to travel domestically and internationally, up to approximately 20%.
Responsibilities
- Lead clinical development strategy and create comprehensive clinical development plans that address worldwide regulatory, clinical, commercial, and patient-access considerations.
- Provide senior clinical and scientific leadership across development programs, ensuring studies are appropriately planned, executed, and delivered within required quality, scope, and timelines.
- Partner closely with cross-functional program teams and execution units to support seamless implementation and high-quality delivery of clinical studies.
- Offer ongoing medical and scientific guidance throughout clinical trial conduct and serve as a senior escalation point for asset-related clinical issues.
- Review, analyze, interpret, and communicate clinical trial data for internal decision-making and external presentations.
- Author, review, and oversee key clinical development documents, including protocols, clinical study reports, Investigator Brochures, and regulatory submissions.
- Build and maintain strong relationships with investigators and key opinion leaders, leading advisory boards and scientific engagements.
- Manage and develop direct reports, including Medical Directors and Clinical Scientists.
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