47 medical-physics "University of California, Santa Barbara" Manager positions at Pfizer

Labeling Operations Manager, Manager

throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external

Manager of Automation Systems

experience in Automation Engineering Experience with process controls equipment; design and debugging skills Broad understanding of systems architecture and operations, and related components Excellent project

Sr Manager Clinical Scientist

ROLE SUMMARY The Senior Manager, Clinical Scientist (CS) will provide medical and scientific study and project support for multiple, global, Phase 1-4 vaccine clinical studies in a clinical program

Senior Manager, Regulatory Affairs CMC

collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. PHYSICAL/MENTAL REQUIREMENTS This position/role works

Manager, Clinician (Non-MD), Early Clinical Development

study teams to meet enrollment and study delivery timelines. The ECS Clinician will work with other functional disciplines as needed (e.g. Research Unit clinicians/Global Clinical Leads/Medical Monitors

Manager, Clinical Scientist

managementplan from a medical/safety/scientific perspective 7) Represents Vaccine Clinical Research and may participate in company-wide, global process improvement initiatives, and champions process enhancements

Labeling Operations Manager, Senior Associate

revising the label. The LOM provides project management to the Labeling Team throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents

Manager, Biostatistics

cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY You will represent Biostatistics on cross

Site Care Partner, Manager

development process, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment Demonstrated success in prior scientific/technical/administrative roles Demonstrated experience

Study Operations Manager II

May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicable Through the Site Care Partner/Country Trial