- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to… more
- AbbVie (North Chicago, IL)
- …scientific research programs; for generating scientific evidence to support medical affairs strategies; and for interacting with regulatory agencies, medical ... must be local to Lake County, IL or Florham Park, NJ Medical Affairs & Health Technology Assessment (MA&HTA) Statistics is responsible for partnering with AbbVie… more
- AbbVie (North Chicago, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible ... to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable… 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 ... governance milestones. o Coordinate cross-functional teams, including clinical development, medical affairs , market access, regulatory , and commercial, to align… more
- AbbVie (Mettawa, IL)
- …matrixed organization, including (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, business insights, OEC, and sales training. This position requires a highly… more
- AbbVie (North Chicago, IL)
- …Immunology Key Stakeholders: PST Lead, Search and Evaluation Team, Project Management, Regulatory Affairs , Discovery, Clinical Operations Qualifications * MD / ... 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. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. + May serve… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …data scientists and data programmers, and external stakeholders including Medical Affairs , Value and Real World Evidence to provide end-to-end statistical expertise ... approve tables, listings and graphs specifications. + Closely work with Medical Affairs to support statistical design, conduct secondary analyses of clinical and… 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. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. + May oversee… more
- AbbVie (North Chicago, IL)
- …with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director , or Director ), in ... Advise internal customers who may contribute to regulated communication on Regulatory /FDA issues including Public Affairs , Clinical Development, Legal, and… more
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