Clinical Trial Manager - Sponsor Dedicated

Fortrea; Thatcham; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Trial Manager in Thatcham, UK. The successful candidate will oversee clinical trials in the UK, Ireland, and the Nordics, managing budgets and ensuring regulatory compliance. Applicants should have 4-5 years of clinical research experience, strong leadership abilities, and a degree in life sciences. This position requires in-office work 50% of the time.

Qualifications

• 4-5 years of experience in Clinical Research.
• Experience in Clinical Trial Operations and leading cross-functional teams.
• Familiarity with ICH-GCP and global regulatory standards.

Responsibilities

• Lead local study team and act as main contact for the Northern European Cluster.
• Manage trial budgets and ensure inspection readiness.
• Develop country-level patient recruitment strategy and risk mitigation.

Skills

Clinical Trial Operations

Leadership

Communication

Time Management

Problem Solving

Risk Management

Education

Degree in life sciences or allied health

Job description

Join Us as a Clinical Trial Manager

Join Us as a Clinical Trial ManagerWe're seeking a Clinical Trial Manager to drive the clinical delivery of research trials with precision and purpose. The role will oversee trials in the UK, Ireland and the Nordics. If you thrive in a fast-paced, collaborative environment and have a passion for clinical excellence - this role is for you!

Location Requirement
This role requires working in the client Uxbridge office 50% of the time.

Key Responsibilities

• Leads local study team and acts as the main point of contact for the Northern European Cluster with the global study team
• Responsible for study oversight and delivery management (time, budget, quality) at country level from start-up to closure.
• Develops country level patient recruitment strategy & risk mitigation
• Leads problem solving and resolution efforts including management of risk, contingencies, issue resolution and escalation to the appropriate stakeholder/s
• Manages trial budgets and vendor coordination
• Ensure inspection readiness of assigned trials within country.

What You Bring

• Minimum 4-5 years of experience in Clinical Research.
• Strong background in Clinical Trial Operations; experience in leading and participating as an active member of cross functional teams,
• Prior CRA experience in the UK (preferred).
• Prior Start Up experience in the UK (preferred).
• Strong organization and time management skills and ability to effectively manage multiple competing priorities
• Excellent leadership, communication and independent decision-making ability.
• Familiarity with ICH-GCP and global regulatory standards.

Qualifications

• Minimum - Degree in life sciences or allied health (or equivalent experience).
• Fluent in English, both written and verbal.

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