CRA II (fixed-term)

Fortrea; Maidenhead; On-site; GBP 28,000 - 42,000; Full time

Job summary

Fortrea is seeking a CRA I or CRA II to support a routine post-market surveillance study within a dedicated FSP model. You will monitor investigator sites across the North of England, build relationships with investigators and site teams, and ensure patient safety, data quality and regulatory compliance.

The role requires travel to Oxford at least once per month and an initial onboarding on-site. A strong commitment to developing your clinical research career is expected.

Qualifications

• CRA I or CRA II with 6–12 months monitoring experience.
• Good understanding of ICH-GCP and clinical trial processes.

Responsibilities

• Monitoring investigator sites across the North of England.
• Building strong relationships with investigators and site teams.
• Ensuring patient safety, data quality, and regulatory compliance.
• Conducting on-site and remote monitoring activities.

Skills

ICH-GCP knowledge

Strong communication

Relationship-building

UK travel

Clinical research mindset

Job description

We are seeking a CRA I or CRA II to support a routine post-market surveillance study within a dedicated FSP model.

Key Responsibilities Include

• Monitoring investigator sites across the North of England.
• Building strong relationships with investigators and site teams.
• Ensuring patient safety, data quality, and regulatory compliance.
• Conducting on-site and remote monitoring activities.

The role requires travel to Oxford at least once per month, as well as an initial onboarding and training period on-site.

About You

• CRA I or CRA II with approximately 6-12 months of monitoring experience.
• Good understanding of ICH-GCP and clinical trial processes.
• Strong communication and relationship-building skills.
• Comfortable travelling regularly within the UK.
• Motivated to continue developing your career in clinical research.

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