Associate Clinical Project Management Director
This is an important and high-profile role within IQVIA. Associate Clinical Project Management Directors drive the delivery of our studies and aid in bringing new therapies to market faster to ultimately improve patients’ lives. It is a position that requires strong vendor management skills and direct liaison across IQVIA functions and with the customer, acting as that accountable point for delivery and quality while maintaining financial control.
As an Associate Clinical Project Management Director you will manage cross functional teams across our global organization. You will be supported by domain experts in every function and enabled by best-in-class technology and data analytics. Key collaborators are the Clinical Lead for site management, the Project Management Analyst for project coordination, tracking and financial analysis and the Site Activation Manager an expert in start-up. IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.
You will need to be comfortable collaborating and communicating with a variety of colleagues and clients and demonstrate flexible and creative leadership. Global experience and a biopharmaceutical, CRO or related vendor (IP supply, clinical laboratory, etc.) is ideal.
While project assignments vary, your typical responsibilities might include:
Serving as the primary project contact with the client
Leading and managing cross-functional project teams
Project status reporting and surveillance for risk
Monitoring team performance against contract and client expectations and according to key performance metrics
Leading problem solving including management of risk and issue resolution
Developing or reviewing study management plans
Managing team resource assignments and accountability
Oversight of database management
Ensuring compliance with study tools, training materials and standard processes, policies and procedures.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor's degree in life sciences or related field and 10 years’ clinical research experience including 6 years’ project management experience and experience in clinical operations; or equivalent combination of education, training and experience.
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Regular sitting for extended periods of time.
May require occasional travel.
At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
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.
IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at firstname.lastname@example.org to arrange for such an accommodation.
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