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Aquestive Therapeutics · 1 month ago

Vice President, Development Operations

Warren, NJ

Full-time

Onsite

Director/Executive

$256K/yr - $305K/yr

15+ years exp

Aquestive Therapeutics is a pharmaceutical company seeking a Vice President of Development Operations. This senior leadership role involves overseeing drug development operations, ensuring alignment with strategic objectives, and managing clinical programs and resources effectively.

Pharmaceutical

Responsibilities

Develop and implement strategies for efficient drug development operations, aligning with corporate objectives and regulatory and quality standards

Responsible for overseeing project management and program deliverables ensuring alignment with the Company’s strategic objectives

Oversee the planning, execution, and monitoring of clinical development programs, ensuring timelines, budgets, and quality standards are met

Ensure robust operations and controls of data management processes, standards, and systems to ensure quality data collection, integrity, storage, management, and analysis

Collaborate with R&D, clinical development, regulatory, quality assurance, and commercial teams to ensure seamless integration of development activities and successful product launches

Manage resources effectively, including staffing, budget allocation, and external partnerships, to optimize development processes and cost management

Ensure all development operations adhere to regulatory requirements and industry best practices, maintaining a strong focus on quality and safety

Establish and monitor key performance indicators (KPIs) to track operational efficiency, project progress, and team performance

Build and lead a high-performing team, fostering a culture of innovation, collaboration, accountability, and continuous improvement

Qualification

Drug development operationsClinical trial operationsRegulatory requirements knowledgeLeadership skillsProject management experienceBudgeting experienceResource allocationCommunication skillsInterpersonal skills

Required

Master's degree in a relevant scientific field or equivalent experience in the pharmaceutical industry

Minimum of 15 years of experience in drug development operations, with at least 7 years in a senior leadership role

Proven track record of successfully managing drug development projects inclusive of clinical trial operations in a CRO model and data management experience

Strong knowledge of regulatory requirements and industry standards related to pharmaceutical development

Excellent leadership, communication, and interpersonal skills, with the ability to influence and drive change at all levels of the organization

Experience in budgeting, resource allocation, and project management tools and methodologies