- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …as a clinical/medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... the following: + Consult with patients or their representatives, clinical, regulatory , and scientific leaders and thoughtfully apply their recommendations… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …as an clinical/medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who will be...following: + Consults with patients or their representatives, clinical, regulatory , and scientific leaders and thoughtfully applies… more
- AbbVie (North Chicago, IL)
- …Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Statistics - Eye Care provides statistical leadership for clinical… more
- AbbVie (North Chicago, IL)
- …as Discovery, Preclinical Development, Clinical Development, Process Development, CMC, or Regulatory Affairs . Must possess solid foundation of generally accepted ... development or marketed. S&E is responsible for conducting all scientific /technical due diligence to ensure an in-depth understanding of...a major revenue driver for the company. The Senior Director , Search & Evaluation will lead the Oncology S&E… more
- AbbVie (North Chicago, IL)
- …support of an overall Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... generate, deliver and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities + Manages the design and… more
- AbbVie (North Chicago, IL)
- …added to our talent pipeline and considered for future opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the ... scientific strategy for pharmacoepidemiology and real-world evidence to support...areas. They will design and interpret studies, contribute to regulatory submissions, and provide expertise in regulatory … more
- Astellas Pharma (Northbrook, IL)
- …modeling, adaptive designs, and hybrid or external controls-to improve efficiency, scientific rigor, and development impact. A key focus is designing studies ... and decision frameworks that balance exploration, safety, and speed with scientific rigor to inform go/no-go decisions and accelerate development. Experience in… more
- AbbVie (Mettawa, IL)
- …matrixed team, which includes (but not limited to): market access, medical affairs , finance, regulatory , legal, supply operations, health economics, clinical ... development, R&D, public affairs , medical and regulatory review, patient relations,...regulatory and compliance guidelines are followed. + Relates scientific detail and clinical study outcomes to impactful communication… more
- AbbVie (Mettawa, IL)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Director , HEOR Strategy, US Access Evidence Strategy and Execution is ... and CMS for the Immunology portfolio. He or she will report into Director , HEOR Strategy, Pan Immunology and Access Evidence Excellence. Responsibilities: + In… more
- Abbott (Abbott Park, IL)
- …groups), as well as R&D Quality Assurance, Procurement, Supplier Quality, Regulatory Affairs , site-level Operations, and outside suppliers/vendors. The ideal ... treatment and management of diseases and other conditions. The position of ** Director Bioconjugation and Organic Chemistry** is within our Process Innovation and… more