Description
At IQVIA, our Clinical Project Managers play a critical role in bringing innovative medicines to patients worldwide. You'll lead the delivery of clinical trials, partnering with sponsors and cross-functional teams to ensure studies are executed efficiently, compliantly and with a focus on quality, timelines and patient impact.
This is an exciting opportunity to lead regional and global clinical studies while expanding your project leadership expertise within one of the world's leading clinical research organizations.
What You'll Be Doing
As a key member of the project leadership team, you'll be responsible for the successful delivery of clinical studies or study workstreams, ensuring projects meet quality, timeline, budget, regulatory and customer objectives.
Key Responsibilities
- Lead the delivery of regional and global clinical studies or assigned study workstreams from start-up through close-out
- Build strong relationships with sponsors, serving as a primary or key project contact and ensuring an exceptional customer experience
- Lead and coordinate cross-functional teams to achieve project milestones and study objectives
- Develop and execute study management plans to support successful study delivery
- Manage study timelines, budgets, quality, risks and operational performance throughout the project lifecycle
- Drive proactive issue resolution, risk mitigation and stakeholder alignment to ensure successful study outcomes
- Support financial oversight, forecasting, change control and vendor management activities where applicable
- Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements, SOPs and contractual commitments
- Contribute to continuous improvement through lessons learned, best-practice sharing and support of developing team members
What We're Looking For
- Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline
- 5+ years of clinical research experience, including project management experience within a CRO, pharmaceutical, or biotechnology environment
- Experience leading clinical studies, study workstreams, or cross-functional project teams
- Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
- Proven ability to manage study timelines, risks, quality, budgets and operational performance
- Experience building effective sponsor and stakeholder relationships within a global environment
- Strong communication, collaboration, problem-solving and decision-making skills
- Ability to thrive in a fast-paced, matrixed environment while balancing multiple priorities
- Passion for advancing clinical research and improving patient outcomes