- AbbVie (North Chicago, IL)
- …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other ... May represent AbbVie at key external meetings. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
- AbbVie (North Chicago, IL)
- …interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other ... to the molecule and disease area; partners with Medical Affairs , Commercial and other functions in these activities as...in the therapeutic area. . Responsible for understanding the regulatory requirements related to the clinical studies… more
- AbbVie (North Chicago, IL)
- …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other ... to augment expertise in the therapeutic area. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
- AbbVie (North Chicago, IL)
- …interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other ... to augment expertise in the therapeutic area. *Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
- AbbVie (Mettawa, IL)
- …or equivalent. 5 years of experience is preferred. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing ... Purpose The Treatment Experience, Insights and Education group within Global Medical Affairs , Oncology aims to reduce barriers to physician acceptance of oncology… more
- AbbVie (Mettawa, IL)
- …business of healthcare policy and managed markets from the perspective of clinical , regulatory , commercial, and policy issues affecting the pharmaceutical and ... working with top national and regional payors + Proficiency with regulatory policies, compliance procedures, clinical / scientific information and ability… more
- Grifols Shared Services North America, Inc (Chicago, IL)
- …for the therapeutic area(s). + Partners with the Medical Directors, National MSL Sr Director , and North America Medical Affairs Sr Director to develop ... and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a...of field medical plans, strategy, and activities within Medical Affairs , as aligned with goals and objectives. This position… more
- Loyola University Chicago (Chicago, IL)
- Director , Office of Registration & Records - HSC Thank you for your interest in Loyola University Chicago. To view open positions, please enter your search criteria ... Full-Time FLSA Status Exempt Campus Maywood-Health Sciences Campus Department Name STUDENT AFFAIRS Location Code STUDENT AFFS-REGIS & RECORDS (06412E) Is this split… more
- AbbVie (Mettawa, IL)
- …promoting best practices and shared learnings. . Cultivate strong relationships with Medical Affairs , Market Access, Regulatory , and Clinical teams to ensure ... + Experience in multiple R&D functions and data domains (eg, preclinical, genomic, clinical , safety, regulatory , real world data, etc.). Considered to have in… more
- AbbVie (Mettawa, IL)
- …functional partners (professional, marketing analytics and business intelligence, CI, PA, medical affairs , medical and regulatory review, OEC, and legal) to ... external media agency + Work with internal cross functional groups (Public Affairs , Professional Marketing, Legal, Regulatory , Medical and Project Management)… more