Manager, Office of Safety Operations (Remote)

Allergan; Lincoln (NE); Remote; USD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a dedicated Manager for the Office of Safety Operations. This pivotal role focuses on enhancing patient safety through effective management of adverse event reporting and compliance with global regulations. You will lead cross-functional teams, drive continuous improvement initiatives, and ensure alignment with regulatory standards. If you have a passion for pharmacovigilance and a collaborative spirit, this opportunity offers a chance to make a significant impact in a dynamic environment. Join a forward-thinking organization committed to innovation and excellence in healthcare.

Benefits

Paid Time Off

Medical/Dental/Vision Insurance

401(k) Plan

Short-term Incentive Programs

Long-term Incentive Programs

Qualifications

• 5+ years in the pharmaceutical industry with 3 years in pharmacovigilance.
• Core knowledge of global pharmacovigilance regulations (ICH, EMA, FDA).

Responsibilities

• Design and implement compliant ICSR pharmacovigilance processes.
• Lead internal audits and external regulatory inspection activities.

Skills

Pharmacovigilance

Regulatory Compliance

Data Analysis

Cross-Functional Collaboration

Training Development

Stakeholder Management

Education

Bachelor's Degree in Science

Tools

Excel

Job description

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 atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

Purpose:

This position supports the Safety Operations organization to achieve its mission of improving patient lives by delivering high quality, and timely adverse event management and through driving industry leading ICSR operations, ICSR standards and technology at AbbVie.

The Manager, Office of Safety Operations sits in the ICSR Compliance department within the Safety Operations function.

This position is responsible for monitoring and ensuring compliance with the global regulatory reporting of ICSRs. The role includes management of investigations to address compliance deviations and drive continuous improvement, as well as managing license partners to ensure alignment on reporting obligations and safety data exchange requirements.

The successful candidate will also support internal and external audits and regulatory inspections by leading in the front room, providing documentation, data analysis, and subject matter expertise related to ICSR processes,

Responsibilities:

• Designs and implements compliant and efficient ICSR pharmacovigilance processes, technologies & training
  Leads improvement of Abbvie’s global clinical and post-marketing case management processes, technology & training
  Implements new ICSR pharmacovigilance legislation into quality systems, metrics, technical requirements & training
• Leads effective cross-functional collaboration with an emphasis on building business relationships with relevant AbbVie stakeholders, including PPS, Commercial, GMA, RDQA, and Affiliates to establish and maintain harmonized ICSR processes
  Leads internal audits and external regulatory inspection activities; supports functional corrective and preventive action investigations
• Supports PPS’ understanding of the changing regulatory environment as it impacts ICSR management, process, technology, and people
  Leverages global data and cross-functional insights to optimize global ICSR operations including design of effective training approaches
  Manages process improvement initiatives with effective change management and rapid solutioning of unanticipated issues
• Manages identification, prioritization, and timely resolution of potentially impactful issues, including clear communication and follow-up across stakeholders through resolution, prevention, and trending
  Responsible as a senior member of the Office of Safety operations team for driving compliance and process business excellence for all ICSR PV activities
• Presents results to senior AbbVie stakeholders. May participate in governance meetings, and maintains strong working relationship with colleagues in PPS, RDQA, and Affiliate PV & Quality organizations
• Develops and manages a team of AbbVie staff to execute the above responsibilities, including coaching/mentoring for staff performance and development (up to 5 people)

This role can be remote in the US.

Qualifications

• Bachelor’s Degree or equivalent in related science field. +5 years pharmaceutical industry experience; including a minimum of 3 years in pharmacovigilance
  Global experience
• Core knowledge of global Pharmacovigilance regulations (ICH, EMA, FDA) and the affiliate environment, with a firm understanding of related quality assurance systems
• Experienced in health authority inspections and/or internal or third-party audits
• Experienced in developing training & quality documents (SOP / Guidelines / CAPAs)
• Skilled in data interpretation; experienced with using excel
• Proficient in case processing processes, procedures, conventions
• Able to influence across stakeholders and manage within a cross-functional matrix; seen as a collaborative partner within the organization
• Able to identify, assess, and effectively manage business and compliance risks
• Experience in leading cross-functional teams preferred
• Established influencing skills

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

• This job is eligible to participate in our short-term incentiveprograms.

• This job is eligible to participate in our long-term incentiveprograms

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent withapplicable 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, visithttps://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