Senior Clinical Project Manager

Services Overview:

· Global/Regional Clinical Trial Leadership: Lead the Study Management Team (SMT) and oversee end-to-end clinical trial delivery, including feasibility, site selection, study start-up, trial execution, database lock, and close-out activities. Serve as a key partner to the Trial Delivery Leader (TDL).

· Cross-functional Stakeholder & Vendor Management: Collaborate with CROs, country teams, and global vendors (e.g., Central Lab, IWRS/IVRS, ePRO), while partnering with Study Responsible Physicians, Data Managers, Supply Managers, and other stakeholders to drive issue resolution and escalation management.

· Project Leadership & Quality Oversight: Accountable for study timelines, enrollment, budgets, documentation, inspection readiness, CAPA management, and GCP compliance. Advanced-level TDMs may lead complex global programs and provide coaching and mentorship to other TDMs.

Education and Experience Requirements:

• 8 years clinical trial management experience in the pharmaceutical industry or CRO. Require 3-4 years of global project management experience. Specific therapeutic area experience.
• Ability to proactively and autonomously identify and preempt budget issues and work with key stakeholders to resolve.
• Strong leadership, project management, stakeholder management, budgeting, and English communication skills are essential.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Deliverables:

• Autonomy in execution of clinical trial management services.
• Depth of knowledge with clinical trial management services.
• Provide coaching/mentoring to less experienced TDMs, if applicable.
• Assumes additional responsibilities or special initiatives such as Champion or Therapeutic Area Expert, as applicable.
• Given assignments that are more complex and/or have a greater potential impact on business results.
• Lead a team of TDMs across a project/program, on insourced and outsourced studies.