Senior Vice President, Clinical Development

Key Responsibilities:

• Provide medical leadership for cross-functional internal workstreams.
• Collaborate with partners in the pharmacovigilance department.
• Lead the writing of clinical and safety sections of key Program documents.

Requirements:

• Proven ability to plan and conduct clinical trials.
• Demonstrated track record in working effectively in cross-functional teams.
• Excellent analytical, problem-solving, and strategic planning skills.

Education:

• MD, DO, or non-US equivalent of MD degree

Work Environment:

• Dynamic, interactive, fast-paced, and entrepreneurial environment
• Domestic or international travel are required