Associate Director, Governance & Operations

The Associate Director, Governance & Operations plays a critical role in enabling compliant, high‑quality execution of Market Access engagements across AstraZeneca’s U.S. business. This position serves as the operational owner and Secretariat of the Advanced Customer Engagement Review Team (ACERT), overseeing governance processes that ensure alignment with regulatory expectations, Fair Market Value (FMV) standards, contracting policies, and internal quality controls.

This role partners deeply with Market Access, Medical Affairs, Commercial, Access Strategy, Compliance, Legal, Finance, Service Strategy, and external vendors to ensure all programs, engagements, and analytics are appropriately evaluated, documented, and executed. In addition, the leader oversees FMV methodologies, program‑level analytics, and CMS Physician Fee Schedule (PFS) rule–aligned documentation, including Reasonable Assumptions and certification requirements.

Accountabilities

• Serve as Secretariat and operational lead for ACERT, ensuring timely, compliant, and high‑quality governance reviews.
• Advise program owners on business proposals and determine the appropriate review complexity and governance pathway.
• Lead the FMV evaluation framework, including oversight of analytic processes, vendor reports, and interpretation of data to support FMV decisions.
• Provide guidance to contracting teams to ensure governance decisions translate into compliant contract execution.
• Maintain robust audit‑ready documentation, including FMV analyses, decision rationales, and approval artifacts.
• Identify opportunities for cost savings through use of FMV tools and leveraging prior FMV reports through vendor
• Oversee governance alignment with CMS PFS rule requirements related to Service Agreements, including certifications and reasonable assumptions documentation.
• Establish and maintain enterprise standards for documenting assumptions used in valuations, cost analyses, and engagement justifications.
• Partner with Legal, Compliance, and business sponsors to ensure all certifications are complete, accurate, and updated in accordance with CMS requirements.
• Conduct training and develop guidance materials to ensure consistent understanding across stakeholders.
• Maintain centralized governance repositories to ensure completeness, accuracy, and readiness for internal/external audits.
• Lead the development, update, and communication of governance processes, systems, policies, templates, training tools, dashboards, and analytic frameworks.
• Provide subject‑matter expertise on Bona Fide Service Fees (BFSF), Anti‑Kickback and Safe Harbor regulations, and other compliance standards.
• Own and manage relationships with external FMV vendors to ensure high‑quality deliverables, clear SLAs, and adherence to governance standards.
  
  

Essential Skills/Experience

• Bachelor’s degree required
• 5 years of experience in pharmaceutical, biotech, Market Access, contracting, compliance, or related field.
• Strong working knowledge of FMV, BFSF criteria, Anti‑Kickback/Safe Harbor principles, and pharma regulations.
• Proven ability to lead cross‑functional governance teams and influence without authority.
• Demonstrated analytical capabilities, including cost modeling, data interpretation, and decision rationale framing.
• Excellent communication, relationship‑building, and critical‑thinking skills.
• High proficiency in MS Excel, PowerPoint, and Word.
  
  

Desirable Skills/Experience

• 5 years of pharma or healthcare industry experience
• Strong project management, leadership, business acumen, and ability to manage multiple priorities, processes, timelines and expectations of multiple stakeholder groups
• Strong interpersonal skills and excellent verbal and written communication skills; able to engage with leadership at all levels of the organization; able to synthesize and concisely communicate team deliverables and accomplishments
• Experience with marketing operations including strategic oversight and execution of speaker bureau programs; strong comprehension of the legal and regulatory landscape in pharmaceutical promotions, pharma industry guidelines, and compliance considerations
  
  

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

AstraZeneca offers the opportunity to shape the future of cancer care by combining scientific rigor with strategic impact in a fast-evolving Oncology environment. Here, medical evidence is translated into real-world practice through close collaboration across Medical Affairs, Commercial and R&D, enabling teams to influence every point in the patient journey. Colleagues are encouraged to test bold ideas, learn from experience and share knowledge across functions, all within a supportive culture that values integrity, openness and continuous development. It is a place where high-performing people see their work directly contribute to advancing a strong pipeline and moving closer to eliminating cancer as a cause of death.

Ready to help transform hematology practice through impactful peer-to-peer education and strategic collaboration? Apply now.

Date Posted

21-Apr-2026

Closing Date

27-Apr-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.