AbbVie

As a Study Management Associate III (Clinical Trial Manager), you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Study Management Associate III (Clinical Trial Manager) works as an independent, contributing member of a cross-functional and global partnership to plan, execute and manage one or more Phase 0-4 clinical trials under the guidance of the Study Project Manager and SMA Manager.

This role is remote-based in Tennessee, Mississippi, Alabama, or Florida. The Associate Director provides educational leadership, inspires a team of Oncology Nurse Educators, and supports nursing education strategies. The AD will collaborate with field leadership and HQ partners on strategy to provide clinically relevant, evidence-based disease state and patient management education in support of safe and effective use of AbbVie products.

The Medical Science Liaison (MSL) is a field based scientific expert that strategically supports the scientific and business objectives of a designated therapeutic area across the product life cycle. MSLs are the primary communicators of AbbVie science within a specific geography with healthcare professionals. MSLs are the field scientific experts on given disease states and treatment options within a designated therapeutic area. They combine strong business acumen, clinical expertise, market awareness, and serve as a conduit of information to a cross functional customer base internally within AbbVie.

The Infrastructure Data Analytics function is an innovative program designed to promote data-driven decision-making and address advanced technology challenges for AbbVie employees. As an Sr. IT Business Data Analyst, you'll explore, analyze, and visualize complex data from diverse sources to identify issues and trends that drive transformation across our global technical landscape. You'll work closely with system owners and business stakeholders to identify areas for improvement.

The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executes multidivisional initiatives. Envisions the future by using global marketplace, technology and business knowledge. Collects and analyzes issues and trends that affect the business.

This person reports into the Therapeutic Area (TA) Director, Global Site Management and is responsible for managing 3 levels of Site Management Leads within a specified Therapeutic Area. Drives a cohesive site management strategy and planning, delivering on Clinical Site Management (CSM) execution plans for specific programs/indications as assigned.

The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations.

Become a key player in our Information Security team as a Senior 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.

The Infrastructure Application Security Architect is responsible for developing and implementing a comprehensive information security program. Key duties include designing secure application architectures, ensuring secure coding and deployment, and defining security policies. This position requires a deep understanding of secure application development practices, API security, and risk identification in system configurations.

This role involves leading Product Safety Teams (PST) and supporting products to ensure the safety profile is monitored and characterized throughout the product lifecycle, including surveillance, signal detection, risk management, and interpreting regulations related to pharmacovigilance to support patient safety activities.

The Medical Science Liaison (MSL) is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle. MSLs are the primary communicators of AbbVie science within a specific geography with healthcare professionals. They combine strong business acumen, clinical expertise, and market awareness.

The AbbVie Insider Risk Lead plays a critical role in safeguarding the organization by monitoring alerts generated from Insider Risk systems, conducting technical investigations, and enhancing detection mechanisms. This role involves analyzing telemetry data to proactively identify potential data loss or insider threats that could impact the business. The Insider Risk Lead will lead the charge in conducting investigations and collaborating with key stakeholders, remediating escalations, and guiding the development of the insider risk program.

As a HTA statistician, you understand all aspects of planning, conducting, and evaluating clinical trials and can develop an HTA strategy. As an expert for all statistics topics, you are part of a cross-functional project team. You plan an HTA strategy and create local analysis plans.

The Clinical Operations Program Director connects science and operations to bring clinical studies to life through the execution of clinical research programs. The Director serves as a strategic advocate for pipeline assets and provides operational reality to our scientific experiments.

This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Aligning DSS study teams with program- and study-level strategies, the role supports governance of assigned programs and studies, both within and outside DSS.

Tasked with implementing the vision and process framework of the CDMSO team by advising employees and teams on executing continuous improvement initiatives. This role coordinates highly effective teams by developing staff and delegating appropriate work assignments and priorities to execute continuous improvement initiatives. Responsibilities include planning and allocating functional resources to achieve objectives while ensuring compliance with GCP and AbbVie SOPs.

This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Uses understanding of clinical trial concepts and cross-functional protocol requirements to execute assigned study assignments. Engages with members of the DSS and cross-functional study teams in order to effectively execute assigned activities. Effectively utilizes available technology to execute assigned activities.

As System Owner responsible for overall delivery inclusive of technical direction, adherence to SLC deliverables, in the development and support of applications and systems by assisting in the preparation of system specifications, testing, and implementation of efficient, cost-effective solutions with different tech stack and architectures spanning N-Tier Architectures and, SaaS space inclusive of Salesforce.

The Associate Director, Regulatory Affairs Devices and Combination Products works with internal and external partners to deliver products to patients, supporting regulatory objectives for the company’s development and marketed device/combination products, including coordination and management of device global submissions. This position focuses on eye care devices and next generational eye care medicinal delivery products.

This role supports the NQPPV Network Lead to fulfil the legal requirements to ensure oversight of AbbVie’s PV system and ensures that National QPPVs (NQPPVs) meet their legal obligations worldwide. The role is the linchpin to a strong & experienced NQPPV Network. Key responsibilities include acting as the primary point of contact for all European NQPPVs.