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
Location: Lake County, IL (AbbVie Headquarters) and open to other AbbVie office locations in the US.
Purpose:
Medical Device Safety Physician leads the safety oversight relevant to her/his assigned products to determine and advise the course of action necessary to meet the safety goals and objectives of specific products and projects. Works in close collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs, medical writing, clinical development, clinical operations, manufacturing, epidemiology, marketing and other functional areas to identify, evaluate, and communicate safety issues. May contribute relevant clinical safety input to new product design teams as needed.
The Medical Device Safety Physician is independently responsible for proactive safety strategy, medical safety assessment of SAE/AEs reported to Product Surveillance, clinical study safety management, contribution to post market surveillance activities, input to compliant regulatory authority reporting, development and implementation of lifecycle safety risk management strategies and communication of safety information for assigned medical device development, clinical studies and marketed products. He/She monitors and manages the ongoing safety profile of products to maximize the understanding of risks and benefits for providers, patients, consumers, study subjects and the environment through proactive review of all relevant pre- and post-marketing safety data, medical analysis and decision making.
Responsibilities:
Device, Combination Products, and InVitro Diagnostics, Clinical Trials- Medical assessment and Management
Responsible for safety aspects clinical trials including drafting and/or review of the Safety Management Plan and relevant safety chapters/text of key clinical trial documents such as informed consent, protocols (specifically inclusion / exclusion criteria, Adverse Event management and reporting, and AEs of interest).
Evaluates all safety data generated in clinical trials on a contemporaneous basis.
Provide medical leadership on global teams on safety related issues.
Responsible for overall evaluation, assurance, and reporting of safety of subjects in clinical trials and clinical development program.
Performs medical assessment of Serious Adverse Events including causality assessment, determination of expectedness, identification of events of interest, sentinel events and additional follow up for pre-and post-marketed products as appropriate.
Provides medical safety input as appropriate to Global Product Teams regarding expectedness, causality, data reconciliation and analysis of safety data.
Review and approve final listings of SAEs, AE, AE of special Interest, and other listings based on the clinical study requirements.
Responds to safety questions from investigator sites and IRBs regarding safety issues and queries.
Provides medical safety interpretation of safety findings for all clinical study reports, including final review of safety relevant adverse event coding for assigned projects and discusses, proposes, and communicates any revision(s) or additions
Contribute to integrated safety summaries, risk/benefit assessments, and other relevant safety sections or documents in support of regulatory submissions and periodic or update reports.
Ensures accurate, relevant, and meaningful CSR data and insights.
Liaises with assigned Data Safety Monitoring Boards.
Responds to safety questions from investigator sites and IRBs regarding safety issues and queries.
Post-market/Product Surveillance Safety
Ensure appropriate assessment of product complaints requiring medical interpretation for assigned products
Ensure appropriate medical assessment and determinations have been documented prior to submission of reports, including MDRs, to regulatory authorities.
Provide medical input and assessment to regular and ad hoc product surveillance and safety reports for publication to regulatory authorities
Provides medical support for reportability decisions and accurate coding for device adverse events and malfunctions
Risk Management & Regulatory support
Contribute to the assessment of newly identified and potential risks for development of risk management plans and risk minimization activities.
Contributes to the development and on-going review/revision of assigned product(s) Clinical Hazards Lists (CHL) and Application Failure Mode and Effects Analysis (aFMEAs)
Reviews device risk management documents such as AE Matrix, Risk Management Plans, Risk Benefit Analysis, Design & process FMEAs, and Risk Management Reports
Participates in Health Product Hazard Assessments and Health Hazard Evaluations
Contribute to writing safety responses to regulatory authorities
Review literature to support submission of new device applications
Review Safety Data Information for Instructions for Use (IFU) to ensure accurate device labeling
New Product (Device, Combo, IVD) Development
Participates as a Core Team Member on New Product Development projects as assigned
SOP Development & Training, Personnel Development
Contributes to the mentoring of colleagues in clinical safety management. Provide technical knowledge to Device Safety Analysts as needed
Develops and maintains comprehensive and current knowledge (e.g., indications, labeling documents, pharmacology, etc.) of the assigned product portfolio and current regulations governing the processing and reporting of safety data, Standard Operating Procedures and Work Instructions
Assist in development of new clinical safety documents as required by clinical studies and assist in updating current Device SOPs
Leads or contributes as an individual to projects / process improvements that support PSEQ's strategic objectives
Qualifications
-MD / DO with 2+ years of residency with patient management experience required
-Prior device safety experience is preferred in addition to MD / DO
-Effectively analyze clinical,post-market, and epidemiological data required
-Effectively write technical documents with direction
-Work collaboratively in a team environment and be self-starting and able to work independently
-Ability to effectively present recommendation/opinions in a group environment
-Fluency, both written and oral, in English
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: $177,000 - $336,000
