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Vice President of Scientific Affairs

2 months ago

San Diego, California, United States PharmaScouts Inc Full time


We present a unique opportunity for a Vice President of Scientific Affairs who is passionate about influencing drug development methodologies and regulatory approvals.

Our organization collaborates with consortia that include industry specialists, healthcare professionals, patient advocacy groups, and regulatory authorities, all committed to accelerating the approval of safe and effective pharmaceuticals across a range of medical conditions.

The VP will take charge of all scientific initiatives and formulate strategies to bolster research and development capabilities. They will ensure the organization’s efficiency, sustainability, and competitive edge through scientific guidance and business acumen.

Key Responsibilities:

Scientific Direction:
Formulate and refine the scientific direction alongside the executive team, managing pre-clinical, translational, and clinical research initiatives.

Research Enhancement:
Strengthen the organization’s research capabilities, maximizing evidence generation and regulatory approval processes.

Portfolio Oversight:
Structure the scientific portfolio for effective knowledge integration and management.

Business Growth:
Identify new business prospects that align with the scientific direction and foster organizational expansion.

Revenue Development:
Establish scientific components of the organizational strategy to create new revenue avenues, including training and talent development.

Leadership Responsibilities:
Guide executive directors, scientific, and administrative personnel across various collaborations.
Attract, nurture, and retain high-performing team members.
Develop systems for consistent, high-quality project management.

Core Duties/Responsibilities:
Evaluate scientific needs and propose solutions for growth and capability enhancement.
Design the scientific value chain for medical product development resources.
Assess the scientific viability of new initiatives.
Translate global medical product development realities into the organization’s framework.
Provide leadership and oversight of scientific endeavors.
Build relationships with regulatory agencies, industry stakeholders, advocacy organizations, and academic partners.
Recruit and assess new scientific talent.
Manage financial oversight of relevant grants or funds for scientific initiatives.

Required Knowledge, Skills, and Abilities:
Educational background in a relevant field.
10 – 15+ years of experience in medical product development and regulatory processes.
In-depth understanding of the drug development and regulatory review process.
Comprehensive scientific, clinical, technical, and regulatory knowledge of medical product development.
Experience with regulatory drug development submissions.
Proficiency in data and quantitative sciences, including clinical pharmacology, statistics, and digital health technologies.
Experience managing matrixed teams and resources.
Strong leadership and strategic planning capabilities.
Ability to facilitate scientific activities among diverse stakeholders.
Knowledge of regulatory pathways and good clinical practices.
Strong management, interpersonal, negotiation, and problem-solving skills.
Expertise in managing complex collaborations and teams.
Adaptability to changing priorities and timelines.
Ability to identify improvement opportunities and implement changes.
Ability to meet deadlines and manage time effectively.
Ability to anticipate and proactively address issues.