[Hiring] Clinical Trial Manager @Parexel

Role Description

We are seeking a local Clinical Trial Manager with oncology experience, to join our team in the UK in a remote capacity. This role is dedicated to a single client and offers the opportunity to play a critical leadership role in delivering country level clinical trials that help advance innovative treatments for patients.

As a local Clinical Trial Manager, you will:

• Lead local study delivery, oversee operational execution, and ensure studies are conducted in compliance with applicable regulations, quality standards, timelines, and budgets.
• Work closely with cross functional teams to drive study performance, support regulatory and ethics submissions, and contribute directly to the successful delivery of clinical research programs.
• Join a fast paced, growth-oriented environment supporting impactful clinical studies for leading biotechnology and pharmaceutical organizations.
• Have opportunities for continued professional development and career growth.

Qualifications

• Strong leadership, team motivation, and stakeholder management capabilities.
• Experience working within clinical research and local clinical trial delivery environments.
• The ability to collaborate effectively across cross functional teams.
• Excellent organizational, time management, and problem-solving skills, with the ability to manage multiple priorities.
• A quality focused approach and commitment to regulatory compliance and study excellence.
• Confidence working with study financial systems, regulatory processes, and clinical trial documentation.

Requirements

• Bachelor's degree or equivalent experience in a relevant scientific, healthcare, or clinical research discipline.
• Minimum of 3 years' experience running local clinical trials.
• Experience in oncology clinical trials.
• Proven ability to lead and motivate cross functional teams to deliver clinical trials on time, within budget, and to required quality standards.
• Good understanding and working knowledge of clinical research, clinical trial phases, ICH-GCP, and applicable country clinical research regulations and guidelines.
• Experience performing submissions to Regulatory Authorities (RA) and Ethics Committees (EC).
• Strong communication, organization, and problem-solving skills.

Preferred Qualifications

• Monitoring experience within oncology clinical studies.
• Experience partnering with study functions to support smooth and effective study delivery.

Benefits

• Medical & Dental Insurance.
• Life Assurance.
• Pension.
• Critical Illness Insurance & Health Screenings.