- Astellas Pharma (Northbrook, IL)
- …the development of product labeling and periodic safety reports, as applicable + Lead scientific review of investigator sponsored research (ISR) proposals in the ... **Medical Lead , Zolbe, MA-US** Do you want to be...company contribution + Company paid life insurance + Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions… more
- J&J Family of Companies (Chicago, IL)
- …needs. The Sr. MSL is considered an established scientific and clinical knowledge lead on current and future J&J Innovative Medicine products per Therapeutic Area ... The Sr. MSL provides research support for company and investigator initiated research. The Sr MSL will function with...+ Demonstrate the ability to partner with others to lead or participate in large scale projects. + Maintains… more
- Merck (Springfield, IL)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
- AbbVie (North Chicago, IL)
- …deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. + ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and… more
- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka ... **(PK)** , **Pharmacokinetics-Pharmacodynamics (PK/PD)** and regulatory submissions. You will lead study design, execution and reporting of **clinical pharmacology**… more
- Astellas Pharma (Northbrook, IL)
- …+ Attends/participates in investigator meetings as needed. + May serve as Lead CSM for specific study providing study level oversight and support for CSMs ... communication and support. The Site Manager will partner with Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study… more
- AbbVie (Mettawa, IL)
- …analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. ... and efficacy of the molecule. As the SD Study Lead , is responsible for oversight of study enrollment and...other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are… more
- AbbVie (North Chicago, IL)
- …deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. + ... analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and… more
- AbbVie (North Chicago, IL)
- …cross-functional teams to develop drug delivery and formulation strategies, lead the design, characterization and understanding of formulations/processes, as well ... candidate will play a crucial role as a project lead within dynamic, engaging, and cross functional teams with...AbbVie policies and procedures. + Understand and adhere to corporate standards regarding code of conduct, safety, and GXP… more
- AbbVie (Mettawa, IL)
- …analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. ... and efficacy of the molecule. As the SD Study Lead , is responsible for oversight of study enrollment and...other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are… more