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Associate Director, Clinical Development Eye Care

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

Responsibilities

  • Prepares scientific reports and presentations using available software and templates.
  • Reviews and contributes to clinical protocols.
  • Utilizes expertise to assist in interpretation of data.
  • Brings together all necessary data and information to prepare internal documents or scientific reports; keep multiple reports moving forward simultaneously (multi-tasking).
  • Coordinates advisory meetings and consulting agreements.
  • Complies with procedures set forth in relevant IQS documents, study protocols, other directives issued by the management regarding clinical/pre-clinical studies.
  • Ensures scientific integrity of all processes.
  • Leads the development of and applies the most current electronic document conventions and processes consistently and accurately.
  • Provides/presents key clinical study information to therapeutic area and management.
  • Committed to producing work of the highest quality.
    Pays close attention to detail.

Qualifications

Qualifications

List required and preferred qualifications (up to 10). Include education, skills and experience.

  • Bachelor's/Master's degree in Science related to field with 11+ years of experience in the pharmaceutical industry or PharmD/PhD with 1+years.
  • Understanding of complex clinical study principles.
  • Possesses good oral and written communication skills.
  • Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters and manuscripts.
  • Team, drug development, and scientific project leadership or related experience.
  • Experience supporting clinical research, drug development and/or therapeutic area operations. Proven record of successful projects brought to completion.
  • Requires multi-faceted, broad-based experience in multiple therapeutic areas or clinical functions. Must have in-depth knowledge of clinical study issues.

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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What You Should Know About Associate Director, Clinical Development Eye Care, AbbVie

At AbbVie, we're on the lookout for an Associate Director in Clinical Development with a focus on Eye Care, located in the beautiful city of Irvine, CA. This role is all about making a difference in the lives of people through innovative medicine. You'll be preparing scientific reports and collaborating on clinical protocols, using your expertise to help interpret complex data. We want someone who thrives on multitasking and can handle several reports at once while ensuring everything meets our high-quality standards. You'll be leading the development and application of electronic documentation that keeps us ahead of the curve in the clinical research field. Communication is key, as you will present important study information to management and stakeholders. If you have the right qualifications, including a bachelor's or master's degree in a relevant scientific field and over 11 years of experience in the pharmaceutical industry, you might be the perfect fit for this pivotal role. Join us at AbbVie and contribute to our mission of addressing some of today's toughest health challenges in the eye care arena!

Frequently Asked Questions (FAQs) for Associate Director, Clinical Development Eye Care Role at AbbVie
What are the responsibilities of an Associate Director, Clinical Development Eye Care at AbbVie?

As an Associate Director, Clinical Development Eye Care at AbbVie, you'll be responsible for preparing scientific reports, reviewing clinical protocols, and coordinating advisory meetings. You'll utilize your expertise to interpret data and ensure that all scientific processes adhere to the highest standards of scientific integrity, while managing multiple reports simultaneously.

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What qualifications are needed for the Associate Director, Clinical Development Eye Care position at AbbVie?

To qualify for the Associate Director, Clinical Development Eye Care position at AbbVie, candidates should possess a bachelor's or master's degree in a relevant scientific field, or a PharmD/PhD with at least one year of experience. Proven experience in the pharmaceutical sector, particularly in clinical research and drug development, is essential.

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How does AbbVie support the growth of the Associate Director, Clinical Development Eye Care?

AbbVie is committed to fostering professional growth for its employees, including the Associate Director, Clinical Development Eye Care. The company offers comprehensive training, mentorship opportunities, and a collaborative work environment where you can lead innovative projects and shape the future of eye care.

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What is the work culture like for the Associate Director, Clinical Development Eye Care at AbbVie?

The work culture for the Associate Director, Clinical Development Eye Care at AbbVie is collaborative and inclusive. The company values innovation and integrity, encouraging employees to bring their best ideas forward while promoting diversity and teamwork within the organization.

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What benefits does AbbVie offer to its Associate Director, Clinical Development Eye Care employees?

At AbbVie, the benefits for the Associate Director, Clinical Development Eye Care include competitive compensation, comprehensive medical/dental/vision insurance, generous paid time off, and participation in both short-term and long-term incentive programs that enhance overall job satisfaction and well-being.

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Common Interview Questions for Associate Director, Clinical Development Eye Care
Can you describe your experience with clinical protocols in eye care?

When answering this question, emphasize your relevant experience with developing and reviewing clinical protocols, specifically related to eye care. Discuss any innovative approaches you've taken and how you've collaborated with teams to ensure successful protocol implementation.

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How do you ensure scientific integrity in your work?

Focus on your attention to detail and commitment to adhering to established clinical guidelines. It's important to mention specific practices you implement to verify the accuracy of data and compliance with regulatory standards.

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Describe a project you've led that successfully brought a drug to completion.

Highlight a specific project, detailing your leadership role, the challenges faced, and the collaborative efforts involved. Discuss the methods you employed to ensure timely completion and the techniques used to navigate challenges.

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What technology do you find most beneficial for analyzing clinical study data?

Discuss your familiarity with various data analysis tools and software that aid in interpreting clinical study data. Provide examples of how these technologies have improved efficiency or the quality of results in your previous roles.

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How do you prioritize tasks when managing multiple reports?

Explain your approach to organization and prioritization. Mention tools or methodologies like time management systems or task management software, and provide examples of how your strategies have led to successful project completion.

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What strategies do you use for keep communication clear among team members?

Describe your methods for ensuring clear communication, such as regular check-ins, utilizing collaborative tools, and encouraging open dialogue within the team to prevent misunderstandings and ensure everyone is aligned.

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How do you stay updated on the latest developments in clinical research and eye care?

Mention specific journals, organizations, and conferences you follow to keep abreast of the latest developments. Discuss how this ongoing learning influences your work and ensures you're employing the most current best practices.

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Can you give an example of a challenging clinical study situation and how you resolved it?

Share a real-life example, outlining the challenge, the actions you took, and the resolution. Emphasize your problem-solving skills and how your interventions led to positive outcomes.

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What motivates you to work in clinical development?

Express your passion for making a tangible impact on patients' lives through innovative therapies. Discuss how working at the intersection of science and patient care drives your motivation.

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What leadership qualities do you believe are essential for an Associate Director?

Discuss key leadership qualities such as communication, empathy, decision-making, and adaptability. Provide examples of how you've demonstrated these qualities in your previous roles and how they contribute to successful team dynamics.

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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, on-site
DATE POSTED
January 6, 2025

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