Overview
In this role you will lead clinical research projects from initiation to completion, ensuring delivery on time, within budget, and to quality standards. You will work within the Functional Solutions team dedicated to a sponsor, collaborating with cross-functional stakeholders to execute studies effectively. You will identify risks, manage issues, and monitor performance and compliance with GCP and sponsor requirements. This opportunity offers growth in a global CRO, with a chance to shape project delivery for impactful therapies and patient outcomes. You will join a values-driven culture that emphasizes collaboration, quality, and sustainability, while operating in a hybrid setup near Slough
Pay / Benefits
- growth opportunities
- collaborative environment
- impactful work improving patient lives
- values-driven culture
- hybrid work arrangement near Slough
Responsibilities
- Lead end-to-end planning, execution, and delivery of clinical research projects within time, budget, and quality targets
- Act as primary sponsor contact and maintain strong relationships across the project lifecycle
- Coordinate cross-functional teams to ensure effective collaboration and execution
- Identify, assess, and mitigate project risks while proactively addressing issues and escalations
- Monitor project performance, resources, deliverables, and financial metrics
- Ensure compliance with regulations, SOPs, GCP, and sponsor requirements
Key requirements
- Bachelor’s degree in Life Sciences or related field
- PM experience within a CRO, biotech, or pharmaceutical environment
- Strong leadership, communication, stakeholder management, and organizational skills
- Proven ability to work independently, manage multiple priorities, and take ownership
- Experience managing timelines, budgets, resources, and risks
- Ability to work in a hybrid environment with on-site days near Slough
- leadership
- communication
- stakeholder management
- project management
- timeline and budget management
- resource management
…