- Sumitomo Pharma (Jackson, MS)
- …a dynamic, highly motivated, and experienced individual for the position of **Senior Manager , Medical Affairs Technology and Digital Innovation** . **Job Duties ... Supports the development, implementation, execution, and oversight of Medical Information/Medical Affairs digital services and innovative digital projects as well as… more
- Veterans Affairs, Veterans Health Administration (Biloxi, MS)
- …Processing Application Coordinator (ADPAC). Manages, monitors, coordinates and provides regulatory guidance on all personnel actions, organizational structures and ... Reviews, interprets and provides recommendations for the revision of regulatory guidelines, policies and standing operating procedures pertinent to personnel… more
- Veterans Affairs, Veterans Health Administration (Jackson, MS)
- …engineering advisor, engineer consultant, engineer designer, contract administrator, project manager , construction coordinator, and instructor during the design and ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus Disease 2019… more
- Takeda Pharmaceuticals (Jackson, MS)
- …and EU standards and guidelines. Serve as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global Device Sub team to ensure that ... represented at the Labeling cross functional teams including clinical, safety, medical affairs , device regulatory and commercial, to ensure highly effective… more
- Sumitomo Pharma (Jackson, MS)
- …and final study reporting. + Collaborate with cross-functional teams, including clinical, regulatory , and medical affairs , to ensure study designs meet ... highly motivated, and experienced individual for the position of **Senior** ** Manager , Biostatistics.** This role will support clinical development programs by… more
- Fujifilm (Jackson, MS)
- …+ Proven track record working with Marketing, Business Development, Engineering/QA, and Regulatory Affairs . + Competitive knowledge of Medical IT and Imaging ... **Overview** The Product Manager is a member of the HCUS/MIPD Solution...US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Edwards Lifesciences (Jackson, MS)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more