- AbbVie (North Chicago, IL)
- …with the CMC Regulatory group. Develop standard processes and lead CMC project teams in planning, preparation, review and approval of sections of CMC submission ... Regulatory and Process R&D. + Partner with CMC Regulatory to assist CMC project teams in...Partner with CMC Regulatory to assist CMC project teams in identifying submission-related risks and develop mitigation… more
- US Tech Solutions (IL)
- **Job Summary:** We are seeking an experienced and motivated HEOR Strategy Associate Director to join our Parkinson's Disease team. You will lead HEOR strategy ... that enhance our product's value proposition. The role demands strong project management, time management, and interpersonal skills to lead cross-functional efforts… more
- AbbVie (North Chicago, IL)
- …including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs, Regulatory Affairs, and Clinical Development (both early and late ... Neuroscience, and Endocrinology. Participants will enter the program as Associate Medical Directors. Responsibilities: + With appropriate supervision, manages the… more
- AbbVie (North Chicago, IL)
- …development of information for reports submitted to the FDA and Global Regulatory Authorities. The successful applicant will monitor adherence to protocols and ... Leader, designs, conducts and reports clinical trials in line with the development, regulatory and commercial strategy. + May lead 0-5 employees in a matrixed… more
- AbbVie (North Chicago, IL)
- …for Immunology Key Stakeholders: PST Lead, Search and Evaluation Team, Project Management, Regulatory Affairs, Discovery, Clinical Operations Qualifications * ... serve as a PSTL under the supervision of the Group Medical Director to translate nonclinical and early clinical safety findings, facilitate benefit-risk decision… more
- AbbVie (North Chicago, IL)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... Oversees project -related education of investigators, study site personnel, and AbbVie...scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. +… more
- WTW (Chicago, IL)
- …companies face a variety of different business, cultural, language and regulatory environments. Our Global Services and Solutions line of business helps ... contacts and local Willis Towers Watson consultants. You will serve as the project manager and day to day communication liaison with our clients, create client… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …the timely execution of statistical and research methodological components to meet project objectives and has a thorough understanding of current requirements for ... statistical expertise and delivery of analyses. + Actively participate in project /study team meetings. Develop statistical sections of protocols; participate in… more
- AbbVie (Mettawa, IL)
- …problem solving within the cross-functional team + Translating TA business into project concepts to develop analysis plans, study design and corresponding analysis + ... to the writing and publishing of scientific presentations + Monitor scientific, regulatory and reimbursement / access trends, events and policies for their potential… more
- Humana (Springfield, IL)
- …and overseeing audit activities to ensure compliance with internal policies, regulatory requirements, and industry standards. The Director Internal Audit ... part of our caring community and help us put health first** The Director , Internal Audit develops, plans and evaluates internal audit programs for the organization's… more