CRA II / SCRA β€” Scotland: Impactful Site Monitoring Expert in Maidenhead

CRA II / SCRA β€” Scotland: Impactful Site Monitoring Expert in Maidenhead

Maidenhead Full-Time 31500 - 38500 Β£ / year (est.) No working from home possible
Fortrea

At a Glance

  • Tasks: Monitor clinical study sites and ensure compliance while supporting patient safety.
  • Company: Fortrea, a growing FSP team in the healthcare sector.
  • Benefits: Collaborative environment with opportunities for professional growth.
  • Other info: Travel to investigator sites required; dynamic role with career advancement potential.
  • Why this job: Make a real impact on patient safety and data integrity in clinical studies.
  • Qualifications: Experience as a CRA II or SCRA1 with strong monitoring skills.

The predicted salary is between 31500 - 38500 Β£ per year.

Fortrea is seeking an experienced CRA II or a SCRA1 to join our growing FSP team.

This opportunity is based in Scotland, working on a variety of clinical studies while developing your expertise in a collaborative environment.

We value the ability to monitor study sites, ensure compliance and support patient safety, data integrity and study quality.

Travel to investigator sites will be required as needed.

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CRA II / SCRA β€” Scotland: Impactful Site Monitoring Expert in Maidenhead employer: Fortrea

Fortrea is an exceptional employer that fosters a dynamic and collaborative work culture in Maidenhead, England. With a strong emphasis on employee growth and development, we offer comprehensive training programs and opportunities for advancement within the pharmaceutical sector. Our commitment to innovation and client success ensures that you will play a pivotal role in shaping the future of healthcare while enjoying a supportive environment that values your contributions.

Fortrea

Contact Details:

Fortrea Recruitment Team

We think you need these skills to ace CRA II / SCRA β€” Scotland: Impactful Site Monitoring Expert in Maidenhead

Site Monitoring
Compliance Assurance
Patient Safety
Data Integrity
Study Quality
Clinical Study Management
Collaboration Skills