cFSP Clinical Project Manager (IVD)
IQVIA
Lexington, Kentucky
project manager
manager
management
lead
manager
financial
project management
cross functional
delivery
data
analytics
team
training
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December 2, 2022
IQVIA
Lexington, Kentucky
(Qualified applicants will have prior experience as global project lead managing global in-vitro diagnostics clinical trials)
The Clinical Project Manager role requires you to manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best-in-class technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up.
This is an important and high-profile role. IQVIA s size and global footprint will present you with the breadth of opportunities necessary to develop your career.
Typically assigned to one or two projects, or a program, responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
The Clinical Project Manager role requires you to manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best-in-class technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up.
This is an important and high-profile role. IQVIA s size and global footprint will present you with the breadth of opportunities necessary to develop your career.
Typically assigned to one or two projects, or a program, responsibilities might include:
- Bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies
- Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
- Serving as the primary contact with the customer for progress and governance
- Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies, and procedures
- Anticipating risk and implementing mitigation strategies
- Managing study team assignments, accountability, and resource requirements
- Ensuring the study budget is managed proactively including scope changes and financial systems are accurate
- Bachelor's degree in life sciences or related field and 5-7 years clinical research experience
- Global project management experience within the drug development industry, with previous CRO experience is ideal. Minimum 4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training, and experience
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
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