- AbbVie (Irvine, CA)
- …objectives, both strategic and applicable regulatory requirements. Director , Safety , Regulatory and Medical Affairs Quality Standards is responsible ... for the management of a RDQA global Safety , Regulatory Affairs (RA) and...role reports to the Senior Director of Safety , Vigilance and Medical Affairs Quality Assurance.… more
- Herbalife (Torrance, CA)
- Director , Global Regulatory Affairs -...**Overview** **THE ROLE:** Reporting to the VP of Global Regulatory & Post-market Safety Affairs , this ... implementation of strategy for multiple complex projects led by the corporate regulatory affairs team, including process improvement for efficiency gain,… more
- AbbVie (Irvine, CA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs , Strategic Labeling is responsible for ... or Microbiology + Preferred Education: Relevant Master's degree preferred. Certification in regulatory affairs a plus + Required Experience: 10+ years… more
- AbbVie (Irvine, CA)
- …What Your New Manager Wants You To Know The Associate Director / Director , Global Body Contouring, Global Aesthetics Medical Affairs (GAMA) is a key ... the GAMA organization. Working under the leadership of the Executive Medical Director , Global Body Contouring, GAMA in partnership with key medical functional teams;… more
- AbbVie (Irvine, CA)
- …Marketing and Sales- Director - Strategic Accounts and their leadership. + Regulatory Affairs ; Legal; OEC. + US Medical Information; Pharmacovigilance. + ... environment, by creating trust and respect with the Medical Affairs field leadership as well as Director (s)-Strategic...Medical Affairs field leadership as well as Director (s)-Strategic Accounts; executes on medical affairs plans… more
- AbbVie (Irvine, CA)
- …core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs , Regulatory Affairs , and Clinical Development ... risk management plans. Responsible for routine and ad hoc safety monitoring reports to regulatory agencies. May...regulatory , etc.) as they relate to ongoing medical affairs projects. May assist as consultant/liaison with other corporations… more
- CSL Plasma (Anaheim, CA)
- …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). **Job...approval to resume donating. + Assures the health and safety of donors participating in the non-red blood cell… more
- J&J Family of Companies (Irvine, CA)
- …various functions including global education, R&D, commercial field leadership, regulatory affairs , clinical affairs , and operations/planning/manufacturing. ... impact health for humanity. Learn more at https://www.jnj.com/. The Senior Director , Global Strategic Marketing will develop and implement the marketing strategy… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is… more
- Edwards Lifesciences (Irvine, CA)
- …life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As ... part of our Clinical Affairs team, you'll hone your scientific curiosity and passion...principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to… more