Global Clinical Label Design & Review Specialist

AbbVie is seeking an experienced professional to independently design, review, and approve study-specific and global clinical labels for worldwide use. You will govern templates, phrase libraries, and regulatory compliance in a validated label design system, driving on-... 

 ...Associate, Regulatory Affairs, Strategic Global Labeling- Operations assists with creation and...  ...including commercial, public affairs, clinical development, legal, quality and others...  ...management within RIM system, labeling document reviews (format and content) and for US drug... 

AbbVie in North Chicago seeks a Senior Clinical Site Management Leader to direct global/area CSM strategy and execution across assigned studies. You will lead site monitors, guide study timelines, and coordinate with the Clinical Study Team to ensure quality, risk management... 

 ...Description The Senior Director, Global Regulatory Strategy Lead and...  ...US regulatory requirements. Reviews regulatory documentation for...  ...competitive data including labeling based on information...  ...regulatory agencies preferred. ~ Clinical foundation preferred with strong... 

Associate I, Clinical Pharmacology Scientific Support & Reporting Full-time Salary Min: 65500 Salary Max: 125500 Workday Global Grade: 14 Compensation: USD 65,500 - USD 125,500 - yearly...  ...blinded efficacy and safety reviews. Responsibilities Prepare scientific... 

 ...safety initiatives across the product lifecycle. You will partner with Clinical Sciences and Global Patient Safety to shape safety decisions, manage governance, and drive risk assessment, labeling, and regulatory discussions. You will coordinate with senior leaders, ensure... 

 ...seeking a Feasibility Manager within Study Feasibility to support global clinical trial operations. You will partner with study teams on design feasibility, country and site selection, protocol reviews, and patient burden assessments to inform recruitment and timelines... 

 ...poster from US Tech Solutions Ensure all promotional materials are reviewed by cross functional teams, medical, regulatory, compliance and...  .... Monitor timelines for material approval as agreed by the Global Materials Review Grid (GRID). Work with Client Global... 

 ...Manager to drive quality excellence across global trials. You will oversee regulatory...  ...readiness and supplier oversight within designated affiliates, reporting to the AREA leadership...  ...quality management, collaboration with clinical development teams, and sustaining One... 

 ...for a talented Junior Digital Designer to join a vibrant, in‑house creative team at a global biopharmaceutical company. This...  ...content experts to interpret complex clinical and scientific data, turning it...  ...UI/UX Designer Portfolio review + creative assessment with... 

 ...approval, and maintenance of global and region-specific medical/technical...  ...core content, summarizes clinical guidelines, and assists in...  ...medical message. Provides review and approval of medical content...  ...states, treatment guidelines, labeling, and relevant internal data... 

 ...XandYouTube. Job Description The Specialist, Strategy Management...  ...is a key contributor on the Global Knowledge Management & Digital...  ...Collaboration (GKMDC) team, supporting Clinical Sciences by leveraging...  ...Management & Digital Collaboration Design, implement, and govern... 

 ...and YouTube. Job Description As Associate General Counsel, Global Alliances Legal, you will join a team of attorneys who support...  ...manufacturing, supply, and commercialization activities. Draft, review, and negotiate amendments, governance documents, dispute... 

AbbVie seeks an experienced Occupational Health Nurse Specialist to advance global work-related health programs, improving employee well-being and...  ...with on-site teams, support on-site and contract health clinics, and collaborate with Legal, Benefits, EHS and HR on health... 

AbbVie is seeking a Senior Manager, RDQA AREA, to lead quality assurance across US Affiliates. The role focuses on proactive quality management, collaboration with RDQA and Affiliate leaders, and achieving first-pass approvals through robust risk-based strategies. Responsibilities...

 ...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps...  ...compelling economic, clinical, and operational evidence...  ...Economics & Outcomes Research Lead designs and oversees a comprehensive...  ...systematic literature reviews, meta-analyses, and indirect... 

 ...YouTube. Job Description The Clinical Operations Program Director...  ..., strategic thinking, a global mindset and innovative solutions...  ...Team and Development Review Committee whose remit is to maximize...  ...complexity of trial designs vs speed) Responsible for the... 

AbbVie in the United States seeks a Manager, Global Portfolio Management to oversee a portfolio of Clinical Sciences projects using standardized PM tools and processes. You will collaborate with team members and stakeholders to address business challenges and drive successful... 

Athletico, a leading physical therapy provider, seeks a Clinic Manager to lead daily clinic operations and patient care. You may onboard staff, train teams, review treatment plans, and engage with the community to improve health and quality of life. Athletico supports teamwork... 

 ...professional to support batch disposition and ensure high-quality clinical supplies aligned with global regulatory standards. The role requires interaction...  ...ensure material availability. Responsibilities include reviewing records, contributing to audits, and implementing... 

 ...our patients. AbbVie’s R&D global trial footprint has been...  ...have significantly increased clinical trials managed from the Affiliates...  .../R&D enterprise within designated countries around the world....  ...countries with ~ periodic reviews of quality and compliance data... 

Graphic Designer Location: Mettawa, IL 60045 - Hybrid (3 days onsite - 2 remote) Contract...  ...at an in-house advertising agency for a global biopharmaceutical company with 30+ leading...  ...in InDesign and Illustrator. Visualize clinical datasuch as line charts, bar charts, and... 

Job Title: Graphic Designer III Location: Mettawa, IL Salary Range: $40-$45 Introduction...  ...at an in-house advertising agency for a global biopharmaceutical company with 30...  ...in InDesign and Illustrator. Visualize clinical data in InDesign and Illustrator. Create... 

 ...pharmacology research, generating PK/PD proposals and driving methods development. You will lead studies, design clinical pharmacology strategies, and collaborate with global teams to advance CPPM goals. The role involves authoring regulatory documents, performing data... 

 ...This position reports into the Clinical Sciences Product Office &...  ...Product Office & Technology and Global Patient Safety functions work...  ..., and assisting with program reviews to ensure regulatory...  ...and assist with benefit-risk, labeling, and regulatory discussions.... 

AbbVie is seeking a Senior/Executive Medical Director to oversee clinical development programs across multiple therapeutic areas. You...  ...development plans with strong clinical leadership. US-based, with global responsibilities and strategic impact. #J-18808-Ljbffr... 

AbbVie in North Chicago, IL is seeking a Senior Manager, Statistics to provide statistical leadership across clinical trials, patient safety, and global medical affairs. You will work with experts to advance medicines to patients. You will conduct statistical analyses,... 

 ...product life cycle. Responsibilities include design of new products, improving existing...  ...web meetings, and in person visits. \n Review project assignments with supervisor to establish...  ...training facility.\n \n \nJoin our global team of over 6,000 colleagues and make a... 

 ...Integrated Evidence, Value & Access, Brand , Label & Regulatory, and Product Presentation &...  ...issues or opportunities arise. •Reviews and analyzes emerging data objectively to...  ...functional environment, preferably with a global scope. •Ability to objectively exercise... 

 ...providing writing support to clinical trial registration and results...  ...and complete information globally. Provides medical writing...  ...objectives. Coordinates the review, approval, and other appropriate...  ...with more complex study designs per global registry requirements...