Program Lead II

Clinical Operations Program Director

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio.

The Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more clinical research programs. The Clinical Operations Program Director serves as a strategic advocate for pipeline assets and provides operational reality to our scientific experiments via scientific expertise, strategic thinking, a global mindset and innovative solutions to address risks and challenges. The Clinical Operations Program Director also serves as an inspiring people leader responsible for developing a pipeline of talent for the Development Operations organization.

Responsibilities include :

Integral member of the Pipeline Commercialization Model's Integrated Evidence Strategy Team and a strategic partner for the Asset Strategy Team and Development Review Committee.

Developing the clinical operational strategy and responsible for the execution of clinical studies / programs.

Responsible for the programmatic evaluation of risks and mitigations.

Interacts with and influences all levels of management and cross-functional team members.

Key contributor to the portfolio planning process.

Reviews and provides clinical operations content to clinical and regulatory documents.

Responsible for overall external budget management.

Leads large scoped, cross-functional innovation and process improvement initiatives.

Responsible for developing, managing, mentoring clinical operations staff.

Responsible for executing clinical programs in compliance with quality standards.

Qualifications include :

Bachelor's degree or equivalent is required, typically in nursing or scientific field. An Associate's degree / R.N. or equivalent with relevant experience is acceptable.

Must have 12+ years of Pharma-related / clinical research related experience.

10 years in clinical research demonstrating a high level of core, technical, and leadership competencies.

Experience in risk management, decision-making, strategic execution.

Good communication skills.

Demonstration of successful coaching, mentoring, and people management.

Considered a subject matter expert in the application of standard business procedures.

Integral participation in initiatives or advancement of strategies for clinical operations.

Experience in successful study initiation through study completion, primary data analysis, and / or in multiple phases of studies.

Additional information :

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical / dental / vision insurance and 401(k) to eligible employees.

This job is eligible to participate in our short-term incentive programs.

This job is eligible to participate in our long-term incentive programs.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.