Job Overview

The clinical project manager in this role will be responsible for overseeing a portfolio of observational studies under one client. It is important for this individual to be familiar with observational research, take initiative, lead and build governance processes with minimal guidance, and have experience managing studies and analyses. This is an important and high-profile role within our Real World Solutions team and IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career. 

Who do you work with?

• Epi and data science leads to understand project specific goals and timelines
• Vendors to communicate status of deliverables and workflow
• Program leads to manage full portfolio of projects

What are you great at?

• Managing execution of high-priority time-critical studies while tracking the progress of the studies
• Driving progress by anticipating issues, identifying gaps/roadblocks, working with stakeholders to solve problems
• Managing a portfolio of studies and communicating updates across multi-disciplinary team
• Coordinating stakeholder forums (internal, committees, vendors)
• Working with an increasing level of autonomy and developing cross-functional collaborations in a matrix environment

Typically assigned to one large portfolio of studies within one therapeutic area, responsibilities might include: 

• 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 portfolio governance structure, ensuring consistent use of study tools, training materials and compliance with standard processes, policies, and procedures 
• Generating project or program level reporting and monitoring metrics for senior management, disseminate reports to relevant stakeholders
• 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 

REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES 

• Bachelor's degree in life sciences or related field  
• Global project management experience within the drug development industry, with previous CRO experience is ideal  
• Minimum 2-4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training, and experience 
• In depth knowledge of real-world evidence study designs 

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.