Clinical Project Manager, IVD

Job Description

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.

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

Ideal Experience

• Candidates with 5-10 years of diagnostic (IVD) clinical trial management experience
• PHCS / CDx experience is highly preferred as well as pathology / tissue diagnostic experience is also preferred
• Strong project management and organizational skills, leadership, teamwork / collaboration, stakeholder management, clear communication skills
• Experience with global studies and IVDR

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• 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

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.

Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.

The potential base pay range for this role, when annualized, is $112,000.00 - $186,600.00. 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.