Associate Clinical Project Management Director, Immunology and Women's Health at IQVIA

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.

The dedicated Immunology and Women's Health 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 Immunology and Women's Health team is growing quickly, and candidates with experience in the following experience can expect to have a strong impact:
 

• Autoimmune and Rheumatology (Lupus, Rheumatoid Arthritis, Osteoarthritis)
• Dermatology (Psoriasis, Atopic Dermatitis or Urticaria)
• Rare Diseases
• Plasma Derived Therapies
• Women’s Health (Fertility; Contraception; Endometriosis or Osteoporosis)

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.

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.