About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job DescriptionThe AbbVie R&D Device and Combination Product Development (DCPD) function provides device development expertise for Aesthetic Devices and Therapeutic Combination Products. Within this space, DCPD is accountable to enable AbbVie’s Early R&D Pipeline by providing support to AbbVie’s clinical cross-functional partners to ensure the successful inclusion of devices and drug delivery systems throughout the entire process.
We are seeking an Associate Director, Clinical Management within the DCPD organization to lead a global team, support initiatives, and prepare for clinical trials involving devices and drug delivery systems. As the strategic and operational leader of the DCPD Clinical Management team, the Associate Director is accountable for setting direction, driving day-to-day operational excellence, and developing and empowering the team to deliver against its mission. You will cultivate a collaborative culture while owning stakeholder engagement across a broad set of cross-functional partners — including clinical operations, clinical supply, clinical development, regulatory, quality, human factors, and device development teams — coordinating efforts to ensure readiness for all phases of clinical trials.
Responsibilities
Represent device and combination product development in cross-functional forums, serving as leader across other stakeholders within the clinical development process.
Lead, develop, mentor, and coach global team, fostering a culture of accountability, collaboration, and learning while proactively sharing knowledge and insights to build functional capability within DCPD.
Champion organizational continuity and continuous improvement — identifying opportunities to enhance processes, and ways of working across the function.
Ensure effective assignment and distribution of project responsibilities in alignment with organizational priorities.
Provide oversight for device and drug delivery system readiness activities across global clinical trials, from study initiation through completion — including coordination with clinical supply, clinical study preparation, complaint handling, and regulatory submissions.
Guide collaboration with human factors, systems engineering, and broader device development teams to design and execute clinical design validation plans within the design controls process.
Support the team with development of administration instructions and training materials used for clinical trials in collaboration with other cross-functional teams, including clinical development, clinical operations, and human factors.
Support reviewing clinical study protocols and reports to ensure alignment across devices and delivery system requirements.
Provide strategic direction and review for device sections of early-stage regulatory submission documents.
- Bachelor’s Degree in Science related field with 16 years of related work; Master’s Degree Science or PharmD with 14 years of related work; or PhD in Science or related field with 8 years of related work experience.
Strong interpersonal and communication skills with the ability to build relationships with diverse internal and external stakeholders across functions.
Demonstrated ability to influence and align cross-functional stakeholders and colleagues across multiple areas of expertise.
Strong track record of people leadership within healthcare, medical device, or pharmaceutical organizations; clinical development experience preferred.
Exceptional problem-solving skills with the ability to navigate scientific and organizational challenges.
Technically proficient with an understanding of the medical device and/or pharmaceutical industry; experience with design control processes preferred.
10% Travel may be required to coordinate between AbbVie sites, third-party suppliers, and/or clinical sites.
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 thisposting 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 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 anduntil 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
Skills Required
- Bachelor's degree in a science-related field with 16 years related work, Master's with 14 years, or PhD with 8 years
- Strong interpersonal and communication skills
- Demonstrated ability to influence and align cross-functional stakeholders
- Proven people leadership experience within healthcare, medical device, or pharmaceutical organizations
- Exceptional problem-solving skills
- Technical understanding of medical devices and/or the pharmaceutical industry
- Clinical development experience
- Experience with design control processes
AbbVie Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.
-
Retirement Support — 401(k) contributions include a dollar-for-dollar match up to 6% plus an additional annual company contribution tied to age and service. Company-paid life insurance and other financial protections further strengthen long-term security.
-
Parental & Family Support — Paid leave programs include up to 12 weeks at 100% for parental leave and separate paid caregiver leave, with eligibility after six months where noted. Adoption and surrogacy reimbursements and family-building resources add further support.
-
Healthcare Strength — Health coverage begins on day one with medical, dental, vision, mental health, and prescription benefits, and preventive care covered at 100%. Options such as HSAs/FSAs and coverage for spouses/domestic partners and children up to age 26 broaden accessibility.
AbbVie Insights
What We Do
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.
