Role Summary
Executive Director, Clinical Science Program Lead (Neuroscience) role leads the Clinical Scientist function, delivering scientific expertise to design and deliver clinical studies and programs. The position leads a team and a complex scope of work to ensure high-quality delivery of innovative protocols and data packages for CSRs and Regulatory Filings, and oversees all clinical studies within assigned program(s).
Responsibilities
- Leads a team or complex scope of work to ensure high quality delivery of innovative protocols and data packages for CSRs and Regulatory Filings
- Oversees all clinical studies within assigned program(s) to ensure consistency across program(s)
- Ensures high quality and timely delivery of protocols and data; implements quality assurance plans
- Maintains an advanced understanding of the status of all trial activities within assigned Program
- Provides scientific and clinical leadership to support the team; provide program/study/therapeutic area/skills training to team members
- Attends Development Team meetings as needed
- Leads resourcing and budget planning activities for team
- Holds accountability for the performance and professional development of Clinical Scientist team
- Leads proactive risk identification and mitigation plans; provides progress reports and risk assessment updates to Sr. Management
- Reviews and approves clinical contributions to all trial documents and abstracts
- Reviews, audits, and presents data and information to internal leaders and external investigators
- Serves as a key cross-functional collaborator; represents the Clinical Scientist function in process improvement initiatives and cross-functional activities
- Collaborates to support incoming asset and/or business development activities (i.e., due diligence)
Qualifications
- Required: 10+ years of experience in clinical science, clinical research, or equivalent; extensive experience and demonstrated proficiency in managing direct/indirect employees and leading teams
Skills
- Expertise in GCP/ICH, drug development process, study design, statistics, clinical operations
- Recognized internally and externally as a functional/technical expert
- Expert in analyzing, interpreting, and presenting data
- Advanced knowledge and skills to help lead program-specific data review, trend identification, data interpretation
- Expertise in indication, therapeutic area, compounds, competitive landscape and health authority requirements
- Ability to act independently to identify/resolve and lead the team toward resolving program-level issues
- Consistently recognized for strong critical thinking, problem solving, and decision making skills
- Advanced oral and written communication skills, including medical writing, presentations to large groups, and facilitation of interactive discussions and 1-on-1 discussions with internal and external thought leaders
- Demonstrated strong leadership presence
- Expert financial acumen
- Commitment to quality
- Adaptable / Flexible
- Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally
- Promotes a culture of scientific excellence, multidisciplinary problem solving, teamwork, consistency, flexibility, execution, quality and effective communication
- Anticipates needs, assesses and manages business and organizational risks
Education
- Degree in Life Sciences (MD, PhD, PharmD, MS, RN or other scientific field preferred)
Additional Requirements
- Travel: Domestic and international travel may be required