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Sr. Clinical Project Manager (Women's & Reproductive Health)

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Job Details
Job Order Number
JC137116746
Company Name
IQVIA
Physical Address

Overland Park, KS 66210
Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

JOB OVERVIEW:

This is an important and high-profile role within IQVIA. Project Leaders (Clinical Project Managers, Senior Clinical Project Managers and 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 a Project Leader focusing on Women’s and Reproductive Health, 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.

The dedicated Internal Medicine unit sits within IQVIA’s global Project Leadership organization; as a member of this group, you will be responsible for delivery of global and/or regional studies and / or critical process and vendor management in a variety of indications. Our Internal Medicine team is growing quickly, and candidates with the following Women’s and Reproductive Health experience can expect to have a strong impact:

+ Infertility

+ Perinatal and preterm conditions

+ Disorders of pregnancy

+ Endometriosis

+ Dysmenorrhea

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 7 years’ clinical research experience including 4 years’ project management experience and experience in clinical operations; or equivalent combination of education, training and experience.

PHYSICAL REQUIREMENTS

+ 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.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™

IQVIA is an EEO Employer – Minorities/Females/Protected Veterans/Disabled

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 workday_recruiting@iqvia.com to arrange for such an accommodation.

At IQVIA, we have a vision. Where every healthcare decision is based on evidence. Where data science and human science come together to improve global health. Where new and creative solutions aren’t just possible – they are expected.

Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare. The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease. We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.


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