- AbbVie (Mettawa, IL)
- …) as they relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions. . Serve as a therapeutic area ... compliance with regulatory and ethical standards. . Collaborate with Regulatory Affairs , Legal, Compliance, and Pharmacovigilance teams to ensure adherence… more
- AbbVie (San Juan, PR)
- …PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities. NB: All clinical ... research / development activities for products under development, and for post approval commitments such as regulatory agency mandated trials, or those intended… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... and interpret safety data from various sources including non-clinical, clinical, post -marketing and scientific literature for assessment of benefit-risk profile… more