AbbVie

As an Network Engineer in AbbVie Business Technology Solutions (BTS), you’ll have opportunities to contribute to the digital transformation of a leading biopharma company, helping to create solutions that impact patients and their communities for the better. Technical expert that will independently identify, engineer, and optimize new data, software, or technology solutions that address critical business needs.

Support regulatory approval of biologics drug substances by authoring Chemistry, Manufacturing, and Controls (CMC) filing content and by leading cross-functional CMC teams throughout Phase 1, Phase 2, and Phase 3 development. Author sections of regulatory documents, including INDs and BLAs, based on relevant source documentation. Partner with subject matter experts in various process development functions to ensure technical information is accurately transcribed into regulatory documents.

The Security Application Solution Architect is a member of the Information Security team and works closely with other members of the team to develop and implement a comprehensive information security program. This includes defining security policies, processes, and standards. We are seeking a highly skilled architect to collaborate with application development teams, ensuring secure design, coding, configuration, and deployment of technology solutions.

Become a key player in our Information Security team as a Principal DevSecOps Engineer, where you will leverage your expertise in application security, security engineering, and software development to support and enhance our inline code testing and reporting processes. This role involves the implementation and administration of application security tooling, integration into CI/CD pipelines, and providing support for development teams using these products and consuming their findings.

The Regional Sales Trainer (RST) is a dedicated in-field training role that supports a Brand or Franchise in the design and delivery of training solutions to a regional sales organization. An RST will be responsible for providing regional / national training, coaching, and support, encompassing field travel, coaching reports, live training, sales meetings, and virtual sessions. This will ensure the sales organization has the knowledge, skills, and confidence to effectively sell products.

This Clinical Safety Analyst supports the Clinical Trial Patient Safety Organization to achieve its mission of evaluating and ensuring the quality of clinical trial patient safety data by consistent and accurate delivery of high-quality relevant and timely data review. Contributes to a culture of process improvement, innovation, and cross-functional teamwork aligning with the company vision and strategies. This position is contributing to world-wide surveillance of clinical trial patient safety data and continuous improvement efforts.

AbbVie is committed to being an industry leader in accelerating the transformation of molecules to medicines to maximize the value for patients and AbbVie. As the Director, Patient Inclusion, you will enhance patient access & integrate global patient insights. Develop business strategy for the creation of global disease area patient and care-partner councils in priority indications to enable direct access to patient voice across R&D. Lead the design and implementation of cross-functional strategic initiatives that embed inclusive patient engagement into R&D decision-making and enterprise processes.

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. 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.

AbbVie is looking for a talented Senior Cyber Security Engineer to join our Cyber Threat Intelligence team. This new role will focus on designing, building, and automating new components of our secrets discovery program. You will leverage strengths in software development, experience in cyber intel/response and capabilities in data analytics to discover, analyze, validate, and escalate exposed secrets both internally and externally.

AbbVie Clinical Data Strategy and Operations is a best-in-class team responsible for generating business value from clinical trials data through execution and innovation. This role ensures successful delivery of program- and study-level accountabilities, developing a deep understanding of clinical technology capabilities and data flow. Responsibilities include supporting technology delivery, tracking timelines, developing reports, collaborating with stakeholders, and maintaining technical knowledge of clinical data systems.

Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Develops in concert with Regulatory Affairs, the appropriate regulatory strategies for product brands.

This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Drive the Overall eCRF Library Development and Maintenance Project. Proactively Identify, Manage and Deliver Individual Components of Library working with various stake holders.

The Study Project Manager II drives the connection between the asset and operational delivery and execution of one or more clinical research studies. Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The SPM brings strategic, asset level thinking and innovative problem solving to study planning and execution.

The Director provides specialist medical and scientific strategic and operational input into core medical affairs activities such as health-care professional and provider interactions; generation of clinical and scientific data, educational initiatives and safeguarding patient safety. Will work closely with sales, marketing, and commercial teams to provide strategic medical input into core brand strategies, and to support medical affairs, marketing activities and market access.

The Senior Director provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives; safeguarding patient safety. Works closely with marketing and commercial teams to provide strategic medical input into core brand strategies. Drives GMA input into and influences the development of asset strategy.

This position reports into the Safety Operations Product Leadership team which is part of the International Strategy & Safety Operations (ISSO) function in Patient Safety. The Sr. Product Manager oversees the accuracy, completeness and timeliness of all Safety Operations scientific activities and deliverables for Oncology and/or focused disease state. The Sr. Product Manager is the point of contact for Product Safety Teams and contextualization of Adverse Event data.

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.

Key Account Executives are in-field positions focused on our top customers including national corporations, division within national retailers, private-equity backed groups and large multi-specialty practices. The Key Account Executive is responsible for developing relationships with C-Suite and functional leaders within our top accounts and collaborating with the accounts to develop customized business plans and strategies to promote AbbVie products. Develop relationships at C-Suite and key functional leaders for Key Accounts Work with Key Accounts, OTC Pharmacy Executives, and brand teams to develop customized business plans and strategies to promote AbbVie products. Act as thought leaders for Key Accounts, and as the "voice of the customer" back to various sales and marketing teams. Collaborate with internal marketing teams to develop tools and materials for best-in-class program execution.

We are searching for an experienced and passionate AEM Engineer to join our Product Development and Engineering Center of Excellence. This engineer will join the AEM architecture and platform team to support our AEM Cloud platform and build a catalog of reusable components and integrations to support global brand sites and digital products for leading Allergan Aesthetics brands.

Proactively seeks out strategic business opportunities with business unit leaders from one or more business areas. Provides advice, assistance and leadership in the planning, procurement, provision, delivery, management, maintenance, and effective business use of information systems. Analyzes business processes; elicits, analyzes, and documents business requirements and identifies alternative solutions.

The Sr Specialist QA IT Systems is responsible for providing direction in quality assurance software validation activities including: reviewing software requirement documents; writing and reviewing validation documents; executing and reviewing validation test cases; and updating departmental procedures. This position ensures that defined software validation practices and procedures are being followed.

The Principal Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents that support the company's objectives. The writer independently writes most clinical and regulatory documents within their remit and works closely with teams on document authoring and content strategies to ensure alignment with project goals. The writer contributes to project management strategies driving toward submission objectives.

The Senior Site Contract Manager will ensure timely execution of Clinical Study Agreements and related agreements. The role involves working with R&D teams, drafting, negotiating, and executing agreements within Fair Market Value and legal requirements. The SSCM functions as a US contract management expert, mentoring colleagues and driving functional improvement projects.