Clinical Program Manager - San Diego, United States - Manpower San Diego

Description

• You will serve as a member of core team(s), providing strategic direction to study teams to meet goals and timelines
• You will interface with representatives from key functional groups including Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical study activities.
• You will work in collaboration with functional leaders to design/implement strategies and track project plans related to study design
• You will drive the full spectrum of the clinical execution from the design phase to close-out in collaborating closely with the study team.
• You will track and manage strategic study operations including KPIs, study timelines, all budgetary and financial information, etc.
• You will coordinate and prioritize activities amongst trials/establish study milestones to ensure timelines are met
• You will recommend and implement innovative ideas to increase efficiency and quality of study management activities
• You will identify and mitigate risks to study implementation, enrollment, conduct, compliance, and completion
• You will drive selection of Contract Research Organizations (CROs) through competitive bid process and other necessary vendors to support study requirements
• You will provide oversight and execution of CRO study deliverables to ensure that objectives are met

Required Skills (top 3 non-negotiables):

Clinical research 5yrs min

Project/program management 2yrs min

Budget management

Nice to have

CRO management

Medical Device

Experience with a Diabetes related company