Senior Director, Strategic Planning and Operations, Oncology Clinical Development

Regulatory Jobs; Chicago (IL); On-site; USD 180,000 - 240,000; Full time

Job summary

AbbVie in the US is seeking a Senior Director, Project Management to lead the long-term portfolio strategy across Therapeutic Areas. You will partner with the TA VP and TEC to optimize asset value and align development plans with the overall TA strategy, driving cross-functional collaboration and decision-making.

In this executive role, you will advise asset development teams, coordinate external collaborations, and guide the use of playbooks to accelerate pipeline progression while ensuring

Qualifications

• Bachelor's degree in a relevant field is required.
• Advanced degree (PharmD, PhD, MD or MBA) is highly preferred.
• 10+ years in pharma/biotech with portfolio/project management experience.

Responsibilities

• Lead TEC agenda and long-term TA strategy with TA VP and TEC members.
• Advise ADTs to align Playbook with TA strategy and targets.
• Partner with Business Development as co-lead of Therapy Assessment Teams.
• Provide input into Disease Opportunity Profiles and TA investment thesis.
• Coordinate external collaborations to advance portfolio value and outcomes.
• Drive planning and portfolio documentation with DSG, Commercial and R&D.

Skills

Leadership

Interpersonal skills

Analytical skills

Communication skills

Education

Bachelor's degree or equivalent

Advanced degree (PharmD, PhD, MD, MBA) preferred

Job description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Purpose

To enable AbbVie’s emergence as a World Class R&D organization, the Senior Director, Project Management, plays a leadership role with the Development TA Vice President (TA VP) and the Therapeutic Executive Committee (TEC) to optimize the value of our portfolio of current and future assets. Under the guidance of the TA VP, the incumbent is responsible for leading development of the long-term strategy (portfolio plan) for the TA; for supporting existing Asset Development Teams (ADTs) in effective utilization of the Asset Playbook discipline to better enable teams to maximize the value of the asset. Achieving these goals requires a combination of excellent interpersonal and collaborative skills, broad strategic thinking, and an ability to synthesize inputs and drive alignment in complex situations.

Responsibilities

• Serves as a core member of the TEC as a strategic partner with TA VP and TEC members, with responsibility for the TEC agenda and areas of focus, driving the overall, long-term TA strategy.
• Advises ADTs across the lifecycle, to ensure application of the Playbook and alignment of the Target Product Profile (TPP) and Development Plan with the TA strategy.
• Partners with Business Development as Co‑lead of Therapy Assessment Teams, and works with Ventures & Early Stage Collaborations to undertake external molecule assessments consistent with TA strategy.
• Provides strategic input into the development of Disease Opportunity Profiles (DOPs), cross‑functional evaluations of potential Discovery initiatives, and the TA investment thesis.
• Coordinates the generation of competitive environment assessments for review at TEC, to turn the data into useful working knowledge for the TEC and disease area in support of the pipeline.
• As appropriate, facilitates identification, evaluation, and implementation of novel tools and technologies (e.g., biomarkers, drug delivery systems, devices and other platform technologies, compliance tools, disease monitoring techniques) that can be employed to improve or accelerate pipeline progression in disease areas of interest.
• In collaboration with relevant functions, drives internal and external stakeholder assessments in order to anticipate changes in the external environment (e.g. regulatory trends, changing payer environment), and to understand the patient journey and levers to improve outcomes.
• Coordinates the conduct and rollup of long‑range strategic planning and portfolio documentation for the TA, working in close collaboration with the Clinical TA VP, Decision Support Group (DSG), Commercial and R&D.
• Works with TA and TEC leaders to identify, prioritize, and nurture external collaborations (consortia, academic and scientific collaborations, key scientific leader advisors, etc.) in areas where we want to further our understanding of disease pathways and mechanisms. Advances our partnerships and alliances for improved outcomes, creating holistic “Total Patient Solutions”.

• Bachelors or equivalent degree required. Advanced degree (PharmD, PhD, MD, MBA) highly preferred.
• Minimum of 10 years (15+ years preferred) of research/development, commercial, project management, portfolio management, business development, or related experience in the pharmaceutical or biotech industry with a track record of expertise in one or more therapeutic areas.
• Recognized team player with proven facilitative leadership skills in a cross‑functional global team environment. Proven performance in a matrix environment with ability to influence and align stakeholders.
• Excellent interpersonal skills. Ability to interact externally and internally to support business strategy.
• Strong analytical skills. Recognized ability to evaluate complex issues from multiple perspectives to ensure that balanced risk assessments are made.
• Excellent oral and written communication skills.

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.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html