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Associate Director, Clinical Pharmacology (Oncology TA) (Hybrid)

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

Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial goals and regulatory requirements for multiple functions. Generates new PK/PD study proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology, PK/PD or regulatory advances, strengths, weaknesses, opportunities and threats, and responds with appropriate new strategies. Consistently demonstrates excellent record of accomplishment of Clinical Pharmacology and business objectives. Leads Clinical Pharmacology/PK/PD aspects of multiple projects. Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management.

Description:

  • Accountable for Phase 1-4 studies design, and clinical pharmacology strategy; acts as the representative for project(s).
  • Executes strategy, lead teams and various data analyses and interpretation by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question).
  • Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, CTDs, label sections, relevant section of investigator brochures, white papers, and other similar documents.
  • Leads clinical pharmacology and biopharmaceutics meetings, serve as Clinical Pharmacology representative at Clinical Strategy Team/Asset Development Team and present at various departmental and cross functional teams such as study teams, Clinical Pharmacology leadership team, Journal club.
  • Drives small teams with members from Clinical Pharmacology functional groups to provide a unified clinical pharmacology position to clinical, CMC and regulatory teams.
  • Authors scientific publications and present at national and international conferences and interact with KOLs/external stakeholders.
  • Conducts due diligence assessments, summarizes results and represents Clinical Pharmacology on business development teams.
  • Represents Clinical Pharmacology at regulatory meetings.

Qualifications

*This position will be required to sit on-site 3 days / week*

  • PhD with typically 4+ years of experience or Pharm D with typically 6+ years of experience in a relevant field, Master’s Degree or equivalent education and typically 12+ years of experience, Bachelor’s Degree or equivalent education and typically 14+ years of experience;(*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
  • Excellent interpersonal skills
  • Ability to interact with functional representatives and KOLs externally and internally and lead team(s)
  • Strategic thinking and enterprise view
  • Proven scientific track record and technical skills to perform the role
  • Key Leadership Competencies:
    • Delivers business results while also positioning AbbVie for long-term success
    • Persistent and resilient finds the way to move good ideas forward
    • Acts respectfully yet courageously
    • Connects unrelated concepts, generates original or unique ideas
    • Influences colleagues to achieve cross-functional alignment
    • Gives full accountability when delegating and accepts full accountability when delegated to by others

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

$135000 / YEARLY (est.)
min
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$120000K
$150000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Associate Director, Clinical Pharmacology (Oncology TA) (Hybrid), AbbVie

Are you ready to take the next step in your career? AbbVie is seeking an Associate Director of Clinical Pharmacology for our Oncology TA, located in beautiful South San Francisco, CA. In this pivotal role, you will be at the forefront of clinical development, responsible for conceptualizing and managing comprehensive Clinical Pharmacology strategies that meet both commercial goals and regulatory requirements for multiple projects. You'll have the opportunity to craft and execute plans for Phase 1-4 studies, driving the design of pivotal PK/PD studies. Your expertise will be essential as you lead discussions with cross-functional teams and contribute to impactful regulatory documents. This role isn't just about strategy; it's about collaboration and innovation, working with teams across various disciplines to align clinical pharmacology positions with business objectives. If you’re passionate about making a difference in patients' lives through groundbreaking research, this might be the perfect opportunity for you. Join us at AbbVie and be part of a mission that is truly transforming lives. Apply today and help us innovate for a healthier tomorrow!

Frequently Asked Questions (FAQs) for Associate Director, Clinical Pharmacology (Oncology TA) (Hybrid) Role at AbbVie
What are the responsibilities of the Associate Director, Clinical Pharmacology at AbbVie?

As the Associate Director of Clinical Pharmacology at AbbVie, your primary responsibilities will include designing Phase 1-4 studies and crafting clinical pharmacology strategies. You will contribute to new PK/PD study proposals, lead data analyses, and create regulatory documents. Additionally, you will represent Clinical Pharmacology at various team meetings and ensure alignment between clinical, commercial, and regulatory objectives, making your role crucial in advancing our oncology initiatives.

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What qualifications are needed for the Associate Director, Clinical Pharmacology role at AbbVie?

To qualify for the Associate Director position in Clinical Pharmacology at AbbVie, candidates typically need a PhD with at least 4 years of experience, or a Pharm D with 6 years of relevant experience. Alternatively, a Master's degree with 12 years, or a Bachelor's degree with 14 years in related fields like PK, PBPK, or Pharmacometrics is acceptable. Strong interpersonal skills and a strategic mindset are also essential for success in this role.

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What is the work environment like for the Associate Director, Clinical Pharmacology at AbbVie?

The Associate Director, Clinical Pharmacology position at AbbVie offers a hybrid work environment, designed to provide flexibility and collaboration. You will spend three days a week on-site, surrounded by a team of passionate professionals dedicated to innovative research in oncology. The culture at AbbVie emphasizes teamwork and supportive leadership, ensuring that you can thrive while making a significant impact in drug development.

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What is AbbVie’s approach to innovation in Clinical Pharmacology?

AbbVie is committed to innovative research in Clinical Pharmacology by leveraging a strong scientific foundation and encouraging creative problem-solving. As an Associate Director, you will have the freedom to explore new strategies and provide insights based on the latest pharmacological advances. This position allows you to implement your ideas within a collaborative framework, driving the development of therapies that address critical health challenges.

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How does the Associate Director, Clinical Pharmacology position contribute to patient health outcomes?

The Associate Director role in Clinical Pharmacology at AbbVie is critical for improving patient health outcomes. By leading the development of pharmacological strategies for oncology therapies, you'll ensure that drug responses are well understood and optimized for effectiveness and safety. Your work in designing robust clinical studies will contribute to the advancement of new treatments, ultimately benefiting patients in need of innovative therapies.

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Common Interview Questions for Associate Director, Clinical Pharmacology (Oncology TA) (Hybrid)
Can you describe your experience with PK/PD study design?

In preparing for this question, you should detail specific projects where you designed PK/PD studies, emphasizing the methodologies used and results achieved. Highlight your ability to integrate scientific principles with practical applications to meet regulatory and commercial objectives.

Join Rise to see the full answer
How do you ensure alignment across different functional groups during a project?

To answer effectively, discuss your strategies for communication and collaboration. You might mention regular cross-functional meetings, clear documentation, or the importance of establishing common goals to unify the team's efforts and enhance project outcomes.

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What strategies do you employ to stay current with scientific advancements in Clinical Pharmacology?

Here, you can talk about your engagement with professional organizations, attending conferences, and staying updated on relevant journals. Illustrate your commitment to continuous learning and how you apply new information to enhance your work at AbbVie.

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Describe a time when you faced a challenge in clinical study management.

Ensure your answer includes a specific example that illustrates your problem-solving skills. Discuss the challenge, how you approached it, and the successful outcome that resulted from your efforts, demonstrating both resilience and strategic thinking.

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How do you approach writing regulatory documents?

In your response, highlight your experience with different types of regulatory documents and your process for ensuring accuracy and compliance. Mention your attention to detail and collaboration with team members to gather necessary information.

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What role do you think Clinical Pharmacology plays in drug development?

Your answer should reflect an understanding of the integral role Clinical Pharmacology plays in translating preclinical findings into clinical applications, emphasizing its contribution to ensuring that treatments are both effective and safe for patients.

Join Rise to see the full answer
How do you handle feedback from KOLs or external reviewers?

In your answer, emphasize your openness to feedback and how you incorporate constructive criticism into your work. Provide an example of using feedback to improve a project or approach.

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What is your experience with team leadership, especially in multidisciplinary settings?

Describe your experience leading diverse teams, emphasizing your leadership style and how you foster collaboration. Highlight situations where your leadership resulted in successful project outcomes or improved team dynamics.

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How do you prioritize competing deadlines or projects?

Discuss your techniques for managing time and prioritizing tasks effectively. You could share methods like using project management tools or setting clear goals to navigate overlapping deadlines successfully.

Join Rise to see the full answer
What do you think are the key competencies for someone in the Associate Director role at AbbVie?

Focus on essential competencies such as strategic thinking, excellent communication skills, a collaborative team player mindset, and a strong scientific acumen. Use your knowledge of AbbVie's values to align your answer with the corporate mission.

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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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February 3, 2025

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