At a Glance
- Tasks: Lead and manage clinical trials from start to finish, ensuring quality and timelines.
- Company: Join a leading global healthcare company dedicated to improving patient outcomes.
- Benefits: Attractive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and career advancement.
- Why this job: Make a real difference in healthcare by managing impactful clinical studies.
- Qualifications: Experience in clinical project management and strong communication skills.
The predicted salary is between 56700 - 69300 £ per year.
IQVIA is seeking an SSO Clinical Project Manager (CPM) to lead day-to-day planning, execution and reporting of assigned studies in the UK, from first site initiation to close-out. You will be the single point of contact for the study team, coordinating with Trial Leads, CRAs and local stakeholders to ensure timelines and quality.
You will drive start-up planning, risk mitigation, data and budget oversight, and cross-functional collaboration to deliver milestones in line with Sponsor SOPs.
Clinical Program Lead: Global Trial Management employer: IQVIA LLC
IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.
