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

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