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Scientific Director, Medical Affairs - Precision Medicine

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 TwitterFacebookInstagramYouTube and LinkedIn

Job Description

*Preferred location is Lake County, IL (hybrid 3 days per week). Will consider remote candidates. 

Purpose

  • Global Medical Affairs (GMA) leader accountable for the creation and oversight of the execution of our Companion Diagnostics (CDx) Global Medical Affairs (GMA) objectives.
  • Oversees GMA CDx activities ensuring seamless communication and execution on Oncology early CDx launch strategies.
  • Provide strategic support to and guidance to the therapeutic area team in developing, aligning, and executing our early CDx strategies with our Oncology pipeline assets strategies.

 

Responsibilities

  • Develop and coordinate the overarching CDx strategy across multiple early oncology assets to ensure optimal launch planning of our assets.
  • Lead the development and implementation of diagnostic strategies for individual assets.
  • Serve as a key member and content expert in the Pipeline Commercialization Model.  Serve as a key member of the Asset Strategy Teams and Integrated Evidence Teams to shape the development and early launch planning of our companion diagnostics for various assets and indications across the oncology pipeline.
  • Build together with clinical development and precision medicine a comprehensive plan to address the evidence, educational, and standard of care gaps and ensure GMA input into the CDx development strategies. 
    • Responsible for understanding the different regulatory requirements across the geographical areas related to clinical studies and accountable for complying with those requirements.
    • May assist with the scientific review, development, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.  Initiate research projects and drive them to completion, resulting in high quality publications.
  • Accountable for the education of AbbVie’s medical teams on our CDx pipeline and ensures a smooth transition of GMA activities from the pipeline CDx team to the relevant go-to-market medical affairs CDx launch teams.
    • Responsible for the development of CDx educational materials and educating affiliate office and in-field teams.
    • Establish and maintain internal and external relationships to facilitate medical activities.
  • Support drafting regulatory documents for biomarker and CDx to enable prospective analysis in phase 1 and phase 2 studies, including investigational use of candidate companion diagnostic (pre-IVD) assays.

 

 

Qualifications

Qualifications

  • Advanced Degree in related science field, (e.g. MS Pharm, PharmD, MD).
  • 10+ years of work experience in the pharmaceutical industry and drug development.  Experience in executional Medical Affairs roles, regulatory, HEOR, pharmacovigilance or clinical development preferred.
  • 5+ years management experience or position requiring ability to influence cross-functionally. 5+ years of significant leadership experience required to manage multifunctional responsibilities preferred.
  • High degree of empathy for the patient and implements tactics that ultimately impact quality of patient care and access to medicines.
  • Motivational approach, open to new ideas and the ability to connect the dots within and across groups and functions
  • Proven leadership skills to form and implement cross-functional matrix teams.  Ability to model performance management leadership behaviors related to the management level
  • Strong credibility and ability to establish and maintain productive relationships with a variety of audiences, including government regulators, the scientific community in both academic and private sector environment and other key stakeholders.
  • Possesses an array of influencing skills with high emotional intelligence and interpersonal savvy. Can lead and inspire teams inside and outside of own organization to deliver on business priorities.
  • Works across the matrix proactively, partnering with people across functional and geographical boundaries while driving to an outcome.  Co-creates strategy with other functions. Gets the team and cross-functional stakeholders energized about the best solution for the broader AbbVie. Manages relationships adeptly.
  • Demonstrated organizational and administrative skills; able to independently manage workload, set personal and team priorities and adjust as needed
  • Role model of strong interpersonal and teambuilding skills; able to create a shared vision and productively manage conflict between team members with diverse interpersonal styles; able to deliver effective coaching and feedback. Remains calm and effective despite challenging situations, complexity, multiple priorities, and ambiguity.

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, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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

$175000 / YEARLY (est.)
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$150000K
$200000K

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What You Should Know About Scientific Director, Medical Affairs - Precision Medicine, AbbVie

Are you ready to take on a pivotal role as the Scientific Director, Medical Affairs - Precision Medicine at AbbVie in Mettawa, IL? At AbbVie, we're devoted to discovering and delivering innovative medicines that address significant health challenges. Your primary focus will be the creation and oversight of our Companion Diagnostics (CDx) global medical affairs objectives, particularly as we dive into early oncology CDx launch strategies. You'll work closely with therapeutic area teams, developing and coordinating CDx strategies that align with the vision for our oncology pipeline assets. By leading the implementation of diagnostic strategies, you'll play a central role in bringing innovative treatments to market. Your expertise will not only support the education of AbbVie’s medical teams but also foster vital relationships with both internal and external stakeholders. This opportunity calls for an advanced degree and over a decade of pharmaceutical industry experience. If you possess strong leadership skills and a passion for patient care, this role could be your next big adventure, whether you're coming from the lab or the boardroom. Join us in our mission to transform lives through science and compassion!

Frequently Asked Questions (FAQs) for Scientific Director, Medical Affairs - Precision Medicine Role at AbbVie
What does a Scientific Director, Medical Affairs - Precision Medicine do at AbbVie?

As a Scientific Director, Medical Affairs - Precision Medicine at AbbVie, you'll oversee and execute Global Medical Affairs objectives pertaining to Companion Diagnostics (CDx). This involves balancing strategic oversight of early oncology launch strategies and providing guidance to therapeutic area teams to align strategies with oncology pipeline assets.

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What qualifications are needed for the Scientific Director, Medical Affairs - Precision Medicine role at AbbVie?

To qualify for the Scientific Director, Medical Affairs - Precision Medicine position at AbbVie, you need an advanced degree in a related field along with over 10 years of experience in the pharmaceutical sector. Significant leadership experience and a deep understanding of medical affairs processes are also essential.

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What is the work environment like for the Scientific Director, Medical Affairs - Precision Medicine at AbbVie?

The work environment for the Scientific Director, Medical Affairs - Precision Medicine at AbbVie is hybrid, with the preferred location being Lake County, IL. This role typically involves collaboration across multiple teams, both in-person and remotely, resulting in a vibrant and flexible workplace culture.

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How can I apply for the Scientific Director, Medical Affairs - Precision Medicine position at AbbVie?

You can apply for the Scientific Director, Medical Affairs - Precision Medicine role at AbbVie through their careers page. Make sure to prepare a detailed resume that highlights your relevant experience in medical affairs, diagnostics, and cross-functional leadership.

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What impact does the Scientific Director, Medical Affairs - Precision Medicine have on patient care at AbbVie?

The Scientific Director, Medical Affairs - Precision Medicine plays a crucial role in impacting patient care by overseeing the development and implementation of diagnostic strategies that ensure patients receive the best treatments possible. Your leadership will help bridge gaps in standard care, enhancing patient access to innovative therapies.

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What skills are essential for the Scientific Director, Medical Affairs - Precision Medicine at AbbVie?

Essential skills for the Scientific Director, Medical Affairs - Precision Medicine role at AbbVie include strong leadership and interpersonal abilities, strategic thinking, and expertise in regulatory requirements. Additionally, emotional intelligence and the ability to influence across functions are vital for success in this position.

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What types of projects will the Scientific Director, Medical Affairs - Precision Medicine be working on?

In your role as the Scientific Director, Medical Affairs - Precision Medicine at AbbVie, you'll work on various projects, including the development of CDx strategies for early oncology assets, coordinating cross-functional teams, and initiating research projects that drive towards high-quality publications.

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Common Interview Questions for Scientific Director, Medical Affairs - Precision Medicine
Can you describe your experience with Companion Diagnostics?

In answering this question, detail your previous roles involving Companion Diagnostics, emphasizing your strategic input and any successful project launches. Discuss how your experiences have equipped you to oversee CDx strategies effectively.

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How do you prioritize tasks and manage multiple projects in a fast-paced environment?

Provide an example of a situation where you successfully managed multiple projects by prioritizing based on urgency and impact. Illustrate your organizational skills and how you adapt to changing priorities.

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What strategies do you use to influence and lead cross-functional teams?

Highlight your proven leadership style and provide specific instances where you successfully influenced outcomes with cross-functional teams. Discuss communication techniques and relationship-building strategies you employ.

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How do you ensure compliance with regulatory requirements in your projects?

Discuss your understanding of regulatory frameworks and your experience in navigating these requirements. Offer an example of how you ensured compliance in previous roles, citing any challenges you faced and how you overcame them.

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What role do you believe education plays in the success of medical affairs?

Share your views on the importance of educating medical teams and stakeholders about Companion Diagnostics. Illustrate how effective education can lead to better patient outcomes and a smoother launch of new therapies.

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Can you provide an example of a successful CDx strategy you have developed?

Prepare to share a detailed example of a CDx strategy you've developed, focusing on the objectives, the steps you took to achieve them, and the outcomes. Emphasize collaboration, innovation, and how it aligned with business goals.

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How do you approach the development of educational materials for medical teams?

Outline your method for developing effective educational materials, including assessing the needs of the audience, ensuring accuracy, and employing engaging formats. Provide an example of materials you've created and their impact on medical teams.

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What measures do you take to maintain productive relationships with external stakeholders?

Discuss your relationship management skills, providing examples of how you've built and maintained relationships with external stakeholders. Highlight techniques you use to foster trust and collaboration.

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How do you stay updated on advancements in oncology and precision medicine?

Share your strategies for continuous learning, including following key publications, attending conferences, or engaging with professional networks focused on oncology and precision medicine.

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Why do you want to work as a Scientific Director, Medical Affairs - Precision Medicine at AbbVie?

Discuss your passion for innovative medicine and patient care, aligning your career aspirations with AbbVie’s mission. Recall specific aspects of AbbVie’s work in oncology that excite you and relate them to your professional journey.

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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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Full-time, hybrid
DATE POSTED
November 27, 2024

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