- Amgen (Washington, DC)
- …team. Join us and transform the lives of patients while transforming your career. ** Clinical Research Medical Sr. Director - Thoracic Oncology** **What you will ... and implement strategies to drive patient enrollment in partnership with clinical operations and medical affairs organizations. + Support cross-functional… more
- Takeda Pharmaceuticals (Boston, MA)
- …experts across the R&D organization, such QS, Research, Biostatistics, Regulatory Affairs , DMPK, Pharm Sci, and Clinical Science providing leadership and ... and empower you to shine? Join us as Senior Director , Quantitative Clinical Pharmacology Lead in our...staff to ensure they value scientific excellence. + Represents Clinical Pharmacology in meetings with global regulatory … more
- Takeda Pharmaceuticals (Lexington, MA)
- …as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial functions + Coordinate interdepartmental ... to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device… more
- Sanofi Group (Cambridge, MA)
- …collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug ... **Job title** : Clinical Research Director , I and I,...ICH guidelines and other regulations + Review documents supporting clinical development such as Investigator's brochure, regulatory … more
- Sanofi Group (Morristown, NJ)
- …collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug ... **Job Title:** Clinical Research Director **Location** : Morristown,...ICH guidelines and other regulations. + Review documents supporting clinical development such as Investigator's brochure, regulatory … more
- Saratoga Hospital (Saratoga Springs, NY)
- …with the Executive Director of Medical Staff, Medical Education and Regulatory Affairs general orientation educational sessions, mock surveys, onsite survey ... Clinical Regulatory Readiness Manager Location: Saratoga...requirements for organizational compliance. + Collaborate with medical staff affairs team to support OPPE clinical review… more
- Takeda Pharmaceuticals (Boston, MA)
- …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... + Experience must include successful development and implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections,… more
- AbbVie (Irvine, CA)
- …to providing the most comprehensive science-based product offerings available. The Director II, Clinical Development will oversee the direction, planning, ... interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other… more
- Takeda Pharmaceuticals (Cambridge, MA)
- … Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory guidance ... you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in...(eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in… more
- AbbVie (Irvine, CA)
- …and AbbVie study staff. + Responsible for understanding and addressing applicable regulatory requirements related to the clinical studies, clinician reported ... interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory… more