Job Details

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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) .

Job Description

Purpose:

The 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 a Project Manager, Clinical Support, to spearhead initiatives to prepare for clinical trials involving devices and drug delivery systems and enable the early-stage pipeline. Collaboration with clinical teams is crucial in this role. You will play an integral part in coordinating efforts between clinical operations, clinical supply, clinical development, regulatory, quality, human factors, and the device development teams to ensure readiness for all phases of clinical trials. These devices are often technically complex, involve multiple sub-systems, interface directly with the patient, and must meet global requirements.

Responsibilities:

• Support clinical trial readiness activities for device and drug delivery systems, working closely with clinical supply, study teams, quality, and regulatory affairs to ensure efficient study initiation and adherence to appropriate standards and compliance.

• Coordinate device-related aspects of global clinical studies, including partnering with quality teams on complaint resolution, managing documentation, and ensuring compliance with regulatory reporting requirements.

• Collaborate with human factors, systems engineering, and device teams to support design validation planning and execution within design control processes

• Assist in the development and review of administration instructions for use in clinical trials. Contribute to the creation and implementation of training materials for clinical site staff and study teams in partnership with clinical development and operations.

• Author, review, or contribute to device sections for early-stage regulatory submissions.

• Advise clinical study teams to ensure appropriate representation and integration of device-related aspects in protocol design.

• Drive continuous improvement initiatives within device clinical management and across cross-functional teams, leveraging insights and feedback to optimize processes and enhance collaboration.

Qualifications

• Bachelor’s Degree or equivalent education and typically 12 years of experience, Master’s Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience.

• Proven experience with medical devices, combination products, or the pharmaceutical industry, including hands-on involvement with design control processes.

• Solid understanding of the pharmaceutical product development lifecycle; prior clinical development experience strongly preferred.

• Excellent interpersonal skills with a demonstrated ability to work collaboratively across functions and build effective relationships both internally and externally.

• Advanced technical writing proficiency and strong verbal and written communication skills.

• Highly adaptable and strong aptitude for identifying innovative approaches to solve problems and support effective decision-making.

• 10% Travel may be required to coordinate between AbbVie sites, third-party suppliers, and/or clinical sites.

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

Salary: $106,500 - $202,500