Clinical Project Management Director (Indication Director)
IQVIA Madrid
Experteer Overview
As a dedicated Clinical Project Management Director (Indication Director), you lead operational delivery for select indications, translating strategy into execution from phase II to submission. You’ll align resources across the program, guide cross-functional teams, and manage risks to ensure timely, quality trial delivery.You act as a key liaison with the customer, driving accountability and a high-performance, innovative culture. You shape operational excellence using IQVIA’s solutions to support strategic outcomes for your indication portfolio.
Compensaciones / Beneficios- Translate project strategy into operational plans
- Oversee integrated study management plans and core project team execution
- Direct study delivery to optimize speed, quality and cost while ensuring standard processes
- Identify systemic issues and implement best practices across programs
- Set and assess performance objectives for core team
- Collaborate across functional groups to support milestones and resolve obstacles
- Monitor progress and proactively report to stakeholders
- Manage large/complex studies or programs and potential portfolio management
- Proactively manage strategic risk and lead problem solving
- Maintain primary customer relationship and coordinate with IQVIA for business development as needed
- Drive consistency of delivery across projects/programs/portfolio
- Build and lead cross-functional teams to support milestone achievement
- Ensure financial success and identify opportunities to accelerate revenue
- Manage scope changes and change control to align with customer needs
- Capture lessons learned and promote continuous improvement
- Support staff development and mentorship of project team members
- Provide input on team member performance and development plans
- Industry experience in Biotech or BioPharma
- Proven track record in indication-level strategy and delivery within CRO/pharma/biotech
- Bachelor’s degree in Life sciences or related field
- Minimum 12 years of industry/clinical research experience with substantial operational leadership in global trials
- Extensive knowledge of clinical development processes, regulatory requirements, and GCP compliance
- Experience in resource forecasting and strategic planning for complex programs
- Viewed as a leading expert by peers
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