- Astellas Pharma (Northbrook, IL)
- …diverse rotations-Clinical Development (12 months), Medical Affairs (6 months), and Pharmacovigilance (6 months), Participants will gain hands-on exposure to key ... working while fostering collaboration across commercial and Medical teams. 1. ** Pharmacovigilance (6 months)** + Develop hands-on experience in safety monitoring and… more
- Astellas Pharma (Northbrook, IL)
- …data scientist to join our Real-World Data Science (RWDS) team. As an Associate Director of RWDS, you will be an analytic researcher informing and conducting ... consumption and partner closely with Development, Medical Affairs, and Pharmacovigilance /Pharmacoepidemiology colleagues in their research. Additionally, you will collaborate… more
- AbbVie (North Chicago, IL)
- …and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Associate Director/Director, Quality Risk Management is a strategic leader within ... which consists of SMEs and risk practitioners across R&D. Responsibilities: The Associate Director/Director, Quality Risk Management is responsible to: + Serve as… more
- AbbVie (North Chicago, IL)
- …and insights to the forefront of decision making via fit-for-purpose solutions. The Associate Director role in Data Science and Analytics is a leadership role and ... advanced analytics techniques like Machine Learning and Artificial Intelligence. The Associate Director, Design Strategy and Engineering leads the UX/UI development… more
- Sumitomo Pharma (Springfield, IL)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The associate ... for INDs, NDAs, and other related documents. + Partner with Drug Safety & Pharmacovigilance to assess the safety profile of compounds. + Maintain a high level of… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... EMA, PMDA, ICH, etc. + General knowledge of global regulations for pharmacovigilance reporting for approved and investigational products. + Confirm list of upcoming… more