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Clinical Project Manager, Immunology and Women's Health

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Primary Location: Durham, North Carolina, United States Additonal Locations: Ann Arbor, MI,USA; Atlanta, GA,USA; Austin, TX,USA; Baltimore, MD,USA; Boise, ID,USA; Boulder, CO,USA; Cambridge, MA,USA; Charleston, SC,USA; Charlotte, NC,USA; Charlottesville, VA,USA; Cheyenne, Wyoming, United States,USA; Chicago, IL,USA; Cincinnati, OH,USA; Dallas, TX,USA; Denver , Colorado, United States,USA; Hartford, CT,USA; Houston, TX,USA; Jacksonville, FL,USA; Kansas City, KS,USA; Lexington, KY,USA; Los Angeles, CA,USA; Madison, WI,USA; Miami, FL,USA; Montreal, Quebec, Canada,CAN; Nashville, TN,USA; New York, NY,USA; Norfolk, VA,USA; Oklahoma City, OK,USA; Omaha, NE,USA; Overland Park, KS,USA; Philadelphia, PA,USA; Phoenix, AZ,USA; Portland, ME,USA; Portland, Oregon, United States,USA; Providence, RI,USA; Raleigh, NC,USA; Reno, NV,USA; Richmond, VA,USA; San Diego, CA,USA; San Francisco , CA,USA; Santa Fe, NM,USA; Savannah, GA,USA; Seattle , WA,USA; Toronto, ON,CAN; Trenton, NJ,USA; Vancouver, British Columbia, Canada,CAN; Washington DC, DC,USA; Wilmington, DE,USA Full time R1235773

Job description

***This is a remote-based role***

IQVIA’s Immunology and Women’s Health Unit is a global team of professionals dedicated to assisting our clients in driving healthcare forward and enabling medical breakthroughs that advance healthcare and patient treatment options around the world.  We are looking for a Project Leader with experience in Autoimmune and Rheumatology, Dermatology, Rare Diseases, Plasma Derived Therapies and Women’s Health experience to join our innovative and dynamic group.

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 while 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 within our Research & Development Operation and 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:

  • 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

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
  • In depth therapeutic knowledge in Autoimmune/Rheumatology (RA, Lupus or Osteoarthritis), Dermatology (Psoriasis, Atopic Dermatitis or Urticaria) ), Rare Diseases Plasma Derived Therapies, or Women’s Health (including Fertility; Contraception; Endometriosis, Osteoporosis) would be an advantage

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

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