- AbbVie (Mettawa, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Scientific Director, Medical Affairs , provides strategic and ... statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + Works with some supervision and guidance. Exercises judgment within… more
- Astellas Pharma (Northbrook, IL)
- …purpose of the Associate Director is to act independently as Lead Safety Statistician (LSS) / Medical Affairs Statistician (MA) / Exploratory Statistician / ... leads large/complex studies or supports marketed products for a safety purpose. + Contributes to regulatory and...for a safety purpose. + Contributes to regulatory and payer dossiers and publications - provides statistical… more
- Rush University Medical Center (Chicago, IL)
- …aspects of clinical research. * May coordinate timely investigator assessment of safety reports. * Proactively identifies regulatory issues and/or variances with ... on the circumstances of each case. **Summary:** This positions provides regulatory support for multiple clinical research studies, which may involve multi-centered… more
- AbbVie (North Chicago, IL)
- …of work may include clinical trials, patient safety , and global medical affairs . The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , or GMA) to create development strategies for… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …study team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of...sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex… more
- Astellas Pharma (Northbrook, IL)
- …expertise. Through three diverse rotations-Clinical Development (12 months), Medical Affairs (6 months), and Pharmacovigilance (6 months), Participants will gain ... global health authority interactions. + Participate in medical monitoring, clinical safety and efficacy data review, and evidence generation strategy creation based… more
- AbbVie (North Chicago, IL)
- …of work may include clinical trials, patient safety , and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , and GMA, etc.) to create development… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- **Overview** The Associate Medical Director will act as the Medical Monitor for Xeris clinical trials, collaborating with cross-functional study teams on clinical ... design and execution. In this role, the individual will oversee study conduct and safety monitoring for assigned trials, spanning Phases 1 through 3, and may also… more
- Exelon (Oak Brook, IL)
- …gas operations, customer service, transmission and substation, distribution system operations, regulatory and external affairs ). + Advanced proficiency in ... people like you who believe in being inclusive and creative, and value safety , innovation, integrity and community service. We are a Fortune 200 company, 19,000… more
- Abbott (Abbott Park, IL)
- …for treatment of vascular disease. As the Specialist in Global Clinical Affairs , considered as highly experienced and knowledgeable resource within the organization ... products under development. * Participates in adverse event reporting and safety responsibilities monitoring. * Coordinates and provides reporting information for… more
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