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Director, Medical Brand Standards - job 2 of 2

Company Description

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. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description

The Director of Medical Brand Standards is responsible for building and leading the Medical Brand Standard capability within Medical Affairs + Health Impact (MHI) organization, including Medical Review, Scientific Platform, CFL (consistent with the FDA-required labeling), SIUU (scientific information on unapproved uses), and other key initiatives worldwide.

This individual will be responsible for collaborating with Therapeutic Area (TA) Scientific and Medical Directors worldwide (US 60% & International 40%), cross-functional teams (e.g., Medical Compliance Excellence, Commercial, Office of Ethics and Compliance (OEC), Legal, Customer Excellence etc.) and senior leaders to develop, align and execute initiatives that advance internal medical capabilities enabling MHI TA performance, with particular attention paid to standards and governance across MHI.  

This individual will report to the Head of Strategic Planning within the Strategy & Innovation organization, and partner closely with Brand Excellence and Operational Standards in serving as an MHI Lead in advancing Brand Scientific/Medical Review Capabilities, adhering to the highest scientific standards.

Responsibilities:

  • Define and lead Medical Review standards worldwide capability, partnering directly with TAs worldwide and across the portfolio to drive impact through innovative and compliant strategies and functional execution aligned to brand strategies.
  • Develop and deliver Medical Review onboarding and ongoing training content in partnership with Leadership and Capabilities Development.  Maintain a network amongst Medical Reviewers for communication of evolving processes, best practices, CFL opportunities, etc.
  • Serve as Medical Review Subject Matter Expert (SME) in enterprise medical/regulatory collaboration meetings to offer enterprise solutions to advancing compliant promotional resources.
  • Work with Medical Compliance & OEC to address any Medical Review performance aps/monitoring trends or risks.
  • Partner with Strategic Resourcing Alignment and MHI TA teams to continually evolve Medical Review resourcing model including collecting and distributing promotional review metrics dashboard to ensure teams are adequately sized relative to this core capability
  • Lead MHI/AbbVie Scientific Platform process and guidance, including optimization and measurement of usage and connectivity to strategy and functional planning/tactics.
  • Collaborate with cross-functional teams across AbbVie, working closely with commercial, therapeutic areas (TA), regulatory, IT, content excellence and other departments to align strategies and initiatives. Foster collaboration and communication to ensure process agility and capability advancement while maintaining compliance. 
  • Serve as a partner to MHI and cross-functional teams to ensure ongoing skill/process development and evolution to ensure future fit medical brand standards capability. 
  • Stay updated on medical regulations and industry trends, keeping abreast of evolving medical regulations, guidelines, and industry trends. Ensure compliance with relevant regulations and share knowledge and insights with the team to propose new strategies and initiatives.
  • Work cross functionally to collaborate where appropriate on internal MHI/Brand capabilities including but not limited to Medical Review, CFL, SIUU, C2, Scientific Platforms, etc.
  • Serve as functional lead within MHI to drive core capabilities and institutional knowledge, ensuring scientific standards for medical review (in-function/non-promotional, and promotional content), CFL interpretation, and other key strategies/initiatives. 
  • Serve as Medical Brand Standards SME/Lead in advancing US Digital Lab & International Omnichannel capabilities, including core claims and material review, in order to effectively scale across all MHI worldwide.    
  • Build and maintain strong and trusted relationships with key senior leaders to advance Medical Review & CFL capabilities as an integral stakeholder and partner in supporting achievement of organizational goals.

Qualifications

  • Advanced degree required (PharmD, DO, PhD, MD, MBA, master’s in science, RN, RPH, or related healthcare professional master’s degree).
  • Minimum 12 years of combined Medical Affairs experience (may include a blend of commensurate commercial experience). Experience in transformation or organization change initiatives and cross- functional experience beneficial.
  • Brand experience required, with demonstrated ability to translate business needs into strategically aligned functional plans. Experience with compliance and governance programs a plus.
  • Demonstrated ability to develop, articulate and negotiate projects and priorities across functions and leadership, without direct authority.
  • Strong tactical execution and project management experience required. Record of successfully developing and implementing enterprise solutions/ capabilities.
  • Excellent interpersonal, communication, executive presence, and relationship building skills required. Customer experience focused, both internally and externally. Ability to Interact with and influence all levels of management and across teams to develop strategies and execute action plans that will achieve the objectives.
  • Excellent implementation, self-management and organizational skills; able to manage workload, set personal and team priorities and adjust as needed; ability to execute or implement deliverables in a timely manner.
  • Strong business acumen: ability to think strategically and translate a strategy to an innovative and implementable plan.
  • Experience in leading in a matrixed environment, across multiple functions, as well as in a virtual setting.
  • Strong problem-solving skills: ability to anticipate and recognize problems, diagnose root causes and take corrective action to prevent recurrence within the team.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • 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​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​

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

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Average salary estimate

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What You Should Know About Director, Medical Brand Standards, AbbVie

Join AbbVie as the Director of Medical Brand Standards and be at the forefront of innovation in the pharmaceutical industry! In this pivotal role, you will lead our efforts in enhancing the Medical Brand Standard capability within AbbVie's Medical Affairs and Health Impact organization. If you're passionate about shaping and maintaining top-notch medical review standards and have the expertise to collaborate with various teams, this position could be your next great opportunity. You'll work closely with global Scientific and Medical Directors and ensure our initiatives not only meet compliance but also drive impactful outcomes in our therapeutic areas. An emphasis on developing training content and fostering collaboration across multiple functions will allow you to put your leadership skills to the test and make a tangible difference in the lives of many. As we strive for excellence, your advanced degree and over 12 years of Medical Affairs experience will position you well to spearhead our initiatives. If you thrive in dynamic environments and are excited to help empower our teams with knowledge and insights, we invite you to explore this exciting opportunity with AbbVie!

Frequently Asked Questions (FAQs) for Director, Medical Brand Standards Role at AbbVie
What are the key responsibilities of the Director, Medical Brand Standards at AbbVie?

The Director, Medical Brand Standards at AbbVie is responsible for building and leading medical review standards worldwide. This includes developing training content, collaborating with therapeutic area teams, and ensuring compliance with medical regulations. The role also involves optimizing the medical review process in alignment with brand strategies to enhance overall performance.

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What qualifications are required for the Director, Medical Brand Standards position at AbbVie?

To qualify for the Director, Medical Brand Standards role at AbbVie, candidates must possess an advanced degree such as PharmD, DO, or MD, along with a minimum of 12 years of Medical Affairs experience. Brand experience and the ability to navigate commercially are essential, as well as strong project management and tactical execution skills.

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How does the Director, Medical Brand Standards contribute to AbbVie's mission?

The Director, Medical Brand Standards plays a crucial role in advancing AbbVie's mission by ensuring that scientific standards are upheld in all medical reviews. By fostering best practices, collaborating with cross-functional teams, and leading compliance initiatives, the Director helps ensure that AbbVie's innovative solutions are both impactful and aligned with regulatory requirements.

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What skills are important for the Director, Medical Brand Standards at AbbVie?

Key skills for the Director, Medical Brand Standards include strong interpersonal and communication abilities, executive presence, and relationship-building skills. Additionally, a strategic mindset, project management proficiency, and problem-solving abilities are vital for successfully conducting initiatives across a matrixed environment at AbbVie.

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What career growth opportunities exist for the Director, Medical Brand Standards at AbbVie?

The Director, Medical Brand Standards at AbbVie can enjoy a variety of career growth opportunities by engaging in cross-functional collaboration, embracing leadership roles in innovative projects, and continuing professional development in the medical field, all while impacting the organization's long-term vision. AbbVie emphasizes career advancement and encourages employees to take on new challenges.

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Common Interview Questions for Director, Medical Brand Standards
Can you describe your experience with developing medical brand standards?

In answering this question, focus on specific projects where you successfully established or enhanced medical brand standards. Highlight your strategic thinking and collaboration with various teams to develop these standards and the impact they had on compliance and operations.

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How do you ensure compliance with medical regulations in your projects?

Discuss your systematic approach to staying updated on the latest medical regulations and guidelines. Provide examples of how you implement these regulations into your projects, ensuring that all initiatives are compliant while driving innovation.

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What strategies would you use to foster collaboration among cross-functional teams?

Emphasize your communication and interpersonal skills as core strengths in building relationships across teams. Suggest specific strategies like regular meetings, shared platforms for collaboration, and engaging stakeholders early in processes to ensure alignment and effective teamwork.

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Describe a time when you managed a compliance issue within your organization.

This is an opportunity to demonstrate your problem-solving skills. Share a specific situation where you identified a compliance issue, the steps you took to address it, and the corrective actions implemented to prevent recurrence, illustrating your leadership and initiative.

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How do you prioritize various projects with tight deadlines?

Talk about your time management and organizational skills. Explain how you use tools or techniques for prioritization, and provide an example where you successfully balanced multiple projects while meeting deadlines, showcasing your ability to remain effective under pressure.

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What role does data play in your decision-making process?

Discuss the importance of data in shaping strategies and making informed decisions. Give an example of how you utilized data analytics in a previous role to guide your decisions and improve outcomes in medical brand standards.

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Can you provide an example of how you’ve improved a process in your previous roles?

Share a specific example of a process you identified as needing improvement, the steps you took to enhance it, and the positive results that followed. Focus on your analytical approach and collaboration with others to implement changes.

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How would you train new team members on medical review practices?

Outline a structured training program you would develop for onboarding new team members. Highlight aspects such as mentorship, resource availability, and hands-on practice, emphasizing how setting the foundation for best practices ensures version control and consistency.

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What is your experience with leading cross-functional projects?

Share specific insights regarding your leadership style in cross-functional projects. Discuss how you navigate diverse team dynamics, maintain alignment on goals, and how you adapt your communication style to meet the needs of various stakeholders.

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How do you keep yourself updated with industry trends and changes?

Discuss the importance of continuous learning in your career. Explain your methods for staying informed, such as attending industry conferences, participating in webinars, and subscribing to relevant journals, showcasing your proactive approach to professional development.

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AbbVie’s mission is to discover and deliver innovative medicines 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: i...

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DATE POSTED
April 23, 2025

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