Description

You will lead clinical development programs for rare diseases and neurological/neuropsychiatric disorders, creating and executing global clinical development plans. You'll ensure optimal planning and implementation of clinical studies, maintain relationships with investigators and thought leaders, and support regulatory interactions to advance compounds from discovery to development.

Requirements

• MD or equivalent required
• Board Certified/Eligible strongly preferred
• 3-5 years of relevant medical/clinical practice, research, or academic experience within pharmaceutical industry
• Experience with medical monitoring, clinical research, and creating development plans
• Established relationships with thought leaders in depression and mood disorders
• Experience in rare disease and/or neurology strongly preferred
• Demonstrated leadership in cross-functional team environments
• Experience interacting with senior leaders and regulatory agencies
• Excellent communication, interpersonal, management, and organizational skills
• Problem solving and conflict resolution abilities
• Ability to engage in open dialogue with stakeholders
• Highly motivated, self-driven and dependable
• Willing and able to travel domestically and internationally

Responsibilities

• Create and execute global clinical development plans
• Ensure optimal planning, implementation and interpretation of clinical studies
• Maintain and build productive relationships with investigators and thought leaders
• Interact frequently with sites to support study awareness and patient recruitment
• Communicate program issues and results to stakeholders
• Support regulatory interactions and submissions
• Provide clinical and scientific expertise for compound development
• Review business development opportunities
• Comply with regulations and company policies